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Each disease is described by a name, synonyms and relevant keywords. Each gene is described by its name in English and its symbol(s). Diseases and genes are cross referenced.
Each disease is also defined by its OMIM number(s), its ICD code(s) and its Orpha number :
- OMIM is the database of mendelian phenotypes and genes created by Dr. McKusick
- ICD-10 is the 10th International Classification of Diseases established by World Health Organisation
- The Orpha number refers to the Orphanet classification of diseases
::Warning
The provided information is based on published scientific articles. Disease profiles are expert-authored and peer-reviewed texts. These general texts may not apply to specific cases, due to the extensive variability of disease expression. Some information may look shocking. It is of the utmost importance to check if the provided information is relevant or not to a specific case.
Information in Orphanet is updated on a regular basis. It may happen that new discoveries are made in between updates and do not yet appear in the disease profile. The date of the last update is always indicated. Professionals are always encouraged to consult the most recent publications before making any decisions based on the information provided.
Orphanet aims to provide rare disease information to healthcare professionals, patients, and their relatives, in order to contribute improving the diagnosis, care and treatment of these diseases. Information in Orphanet is not intended to replace professional health care.
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1624 Result(s)
- AAA syndrome
- AADC deficiency
- AAE
- AAE 2
- AAE II
- Aagenaes syndrome
- AAOR
- Aarskog-like syndrome
- Aarskog-Ose-Pande syndrome
- Aarskog-Scott syndrome
- Aarskog syndrome
- Aase-Smith II syndrome
- Aase-Smith I syndrome
- Aase-Smith syndrome
- Aase syndrome
- ABCB4 gene mutation-associated cholelithiasis
- ABCD syndrome
- Aberfeld syndrome
- Abetalipoproteinemia
- Ablepharon macrostomia syndrome
- Abnormal number of coronary ostia
- Abnormal origin of the pulmonary artery
- Abnormal origin or aberrant course of coronary artery
- ABPA
- Abruzzo-Erickson syndrome
- ABSD
- Absence deformity of leg - cataract
- Absence of brachiocephalic vein
- Absence of dermatoglyphics - congenital milia
- Absence of fingerprints
- Absence of fingerprints - congenital milia
- Absence of innominate vein
- Absence of pulmonary valve - Fallot's tetralogy - absence of ductus arteriosus
- Absence of pulmonary valve - ventricular septal defect - persistent ductus arteriosus
- Absence of the pulmonary artery
- Absence of the superior caval vein
- Absence of the superior vena cava
- Absence of the SVC
- Absence of tibia
- Absence of ulna and fibula
- Absence of vagina
- Absent foot
- Absent foot, bilateral
- Absent foot, unilateral
- Absent hand
- Absent hand, bilateral
- Absent hand, unilateral
- Absent patellae - scrotal hypoplasia - renal anomalies - facial dysmorphism - intellectual deficit
- Absent thumb - short stature - immunodeficiency
- Absent tibia - polydactyly
- Absent tibia - polydactyly - arachnoid cyst
- Acalvaria
- Acanthamoeba keratitis
- Acanthokeratolytic verrucous nevus
- Acanthoma of the nail matrix
- Acanthosis nigricans
- Acanthosis nigricans - Insulin resistance - muscle cramps - acral enlargement
- Acatalasemia
- Accelerated skeletal maturation - peculiar facies - failure to thrive
- Accessory breasts
- Accessory mitral valve tissue
- Accessory pancreas
- Accessory tricuspid valve tissue
- ACCV
- Aceruloplasminemia
- Acetazolamide-responsive congenital myotonia
- Acetazolamide-responsive myotonia
- ACFS
- Achalasia - addisonianism - alacrima syndrome
- Achalasia-alacrimia syndrome
- Achalasia - microcephaly
- Acheiria
- Acheiria, bilateral
- Acheiria, unilateral
- Acheiropodia
- Acheiropody
- Achondrogenesis
- Achondrogenesis, Houston-Harris type
- Achondrogenesis, Langer-Saldino type
- Achondrogenesis, Parenti-Fraccaro type
- Achondrogenesis type 1A
- Achondrogenesis type 1B
- Achondrogenesis type 2
- Achondroplasia
- Achondroplasia and Swiss-type agammaglobulinemia
- Achondroplasia - severe combined immunodeficiency
- Achromatopsia
- Acid beta-glucosidase deficiency
- Acid phosphatase deficiency
- Acitretin embryofetopathy
- Ackerman dermatitis syndrome
- Ackerman syndrome
- Aconitase deficiency
- Acoustic neurilemoma
- Acoustic neurinoma
- Acoustic neuroma
- ACPS 2
- ACPS 4
- ACPS III
- ACPS with leg hypoplasia
- Acquired adult-onset immunodeficiency
- Acquired aneurysmal subarachnoid hemorrhage
- Acquired angioedema
- Acquired angioedema type 1
- Acquired angioedema type 2
- Acquired angioneurotic edema
- Acquired angioneurotic edema type 1
- Acquired angioneurotic edema type 2
- Acquired bradykinine-induced angioedema
- Acquired C1 inhibitor deficiency
- Acquired CDI
- Acquired central diabetes insipidus
- Acquired ciliary dyskinesia
- Acquired cutis laxa
- Acquired epidermolysis bullosa
- Acquired generalized lipodystrophy
- Acquired Gronblad-Strandberg-Touraine syndrome
- Acquired HbH disease
- Acquired hemoglobin H disease
- Acquired hemophilia
- Acquired hypertrichosis lanuginosa
- Acquired hypoprothrombinemia
- Acquired ichthyosis
- Acquired idiopathic sideroblastic anemia
- Acquired kinky hair syndrome
- Acquired lipoatrophic diabetes
- Acquired myasthenia
- Acquired neurogenic diabetes insipidus
- Acquired neuromyotonia
- Acquired non histamine-induced angioedema
- Acquired porencephaly
- Acquired primary erythocytosis
- Acquired prothrombin deficiency
- Acquired pseudoxanthoma elasticum
- Acquired PXE
- Acquired rippling muscle disease
- Acquired secondary erythrocytosis
- Acquired secondary polycythemia
- Acquired thrombotic thrombocytopenic purpura
- Acquired thrombotic thrombocytopenic purpura due to anti-ADAMTS 13 antibodies
- Acquired Von Willebrand disease
- Acquired Von Willebrand syndrome
- Acral dysostosis with facial and genital abnormalities
- Acral dystrophic epidermolysis bullosa
- Acral persistent papular mucinosis
- Acral self-healing collodion baby
- Acral SHCB
- Acrania
- Acrocallosal syndrome
- Acrocapitofemoral dysplasia
- Acro-cardio-facial syndrome
- Acrocephalopolydactylous dysplasia
- Acrocephalopolydactyly
- Acrocephalopolysyndactyly type 2
- Acrocephalopolysyndactyly type 3
- Acrocephalopolysyndactyly type 4
- Acrocephalosyndactyly type 1
- Acrocephalosyndactyly type 3
- Acrocephalosyndactyly type 5
- Acro-cephalo synostosis
- Acrocraniofacial dysostosis
- Acro-dento-osteo-dysplasia
- Acrodermatitis continua suppurativa of Hallopeau
- Acrodermatitis enteropathica, zinc deficiency type
- Acro-Dermato-Ungual-Lacrimal-Tooth syndrome
- Acrodysostosis
- Acrodysostosis with multiple hormone resistance
- Acrodysplasia
- Acrodysplasia scoliosis
- Acrofacial dysostosis, Catania type
- Acrofacial dysostosis, Genee-Wiedmann type
- Acrofacial dysostosis, Kennedy-Teebi type
- Acrofacial dysostosis, Palagonia type
- Acrofacial dysostosis, Rodriguez type
- Acrofacial dysostosis, Weyers type
- Acro-fronto-facio-nasal dysostosis
- Acrofrontofacionasal dysostosis type 2
- Acrofrontofacionasal syndrome type 2
- Acrogeria
- Acrogeria, Gottron type
- Acrokeratoelastoidosis of Costa
- Acrokeratosis of Bazex
- Acrokeratosis paraneoplastica
- Acrokeratosis verruciformis of Hopf
- Acromegaloid facial appearance syndrome
- Acromegaloid facies - hypertrichosis
- Acromegaly
- Acromegaly - cutis verticis gyrata - corneal leukoma
- Acromelanosis
- Acromelic frontonasal dysplasia
- Acromesomelic dwarfism
- Acromesomelic dysplasia, Brahimi-Bacha type
- Acromesomelic dysplasia, Grebe type
- Acromesomelic dysplasia, Hunter-Thomson type
- Acromesomelic dysplasia, Maroteaux type
- Acrometageria
- Acromicric dysplasia
- Acroosteolysis dominant type
- Acro-oto-ocular syndrome
- Acro-pectoral syndrome
- Acro-pectoro-renal dysplasia
- Acropectorovertebral dysplasia
- Acropigmentation of Dohi
- Acrorenal defect - ectodermal dysplasia - diabetes
- Acro-renal-mandibular syndrome
- Acro-renal-ocular syndrome
- Acrorenal syndrome
- ACRP syndrome
- ACS
- ACS 1
- ACS 3
- ACS 5
- ACTH-independent macronodular adrenal hyperplasia
- ACTH resistance
- Actinic lichen planus
- Actinic LP
- Actinic prurigo
- Actin myopathy
- Action myoclonus - renal failure syndrome
- Activation-induced cytidine deaminase deficiency
- Acute ackee fruit intoxication
- Acute adrenal failure
- Acute adrenal insufficiency
- Acute adrenocortical insufficiency
- Acute and disseminated Langerhans cell histiocytosis
- Acute annular outer retinopathy
- Acute basophilic leukemia
- Acute bilateral depigmentation of the iris
- Acute biphenotypic leukemia
- Acute brachial plexus neuritis
- Acute disseminated encephalitis
- Acute disseminated encephalomyelitis
- Acute encephalitis with refractory repetitive partial seizures
- Acute erythroid leukemia
- Acute fatty liver of pregnancy
- Acute febrile neutrophilic dermatosis
- Acute generalized exanthematous pustulosis
- Acute graft versus host disease
- Acute hepatic failure
- Acute hepatic porphyria
- Acute idiopathic demyelinating polyneuropathy
- Acute infantile liver failure due to mitochondrial DNA-encoded proteins synthesis defect
- Acute infantile liver failure due to mtDNA-encoded proteins synthesis defect
- Acute inflammatory demyelinating polyradiculoneuropathy
- Acute inflammatory polyneuropathy
- Acute intermittent porphyria
- Acute interstitial pneumonia
- Acute interstitial pneumonitis
- Acute intoxication blighia sapida
- Acute leukemia of ambiguous lineage
- Acute leukemia of indeterminate lineage
- Acute liver failure
- Acute lung injury
- Acute lymphoblastic leukemia
- Acute lymphoblastic leukemia/lymphoma
- Acute lymphocytic leukemia
- Acute megakaryoblastic leukemia
- Acute megakaryoblastic leukemia in Down syndrome
- Acute megakaryoblastic leukemia without Down syndrome
- Acute monoblastic leukemia
- Acute monocytic leukemia
- Acute motor axonal neuropathy
- Acute motor-sensory axonal GBS
- Acute motor-sensory axonal Guillain-Barré syndrome
- Acute motor-sensory axonal neuropathy
- Acute multiple sclerosis, Marburg type
- Acute multiple sclerosis, Marburg variant
- Acute myeloblastic leukemia type 1
- Acute myeloblastic leukemia type 2
- Acute myeloblastic leukemia type 3
- Acute myeloblastic leukemia type 5
- Acute myeloblastic leukemia type 6
- Acute myeloblastic leukemia type 7
- Acute myeloblastic leukemia with maturation
- Acute myeloblastic leukemia without maturation
- Acute myelodysplasia with myelofibrosis
- Acute myelofibrosis
- Acute myelogenous leukemia
- Acute myeloid leukemia
- Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor
- Acute myeloid leukemia with 11q23 abnormalities
- Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
- Acute myeloid leukemia with CEBPA somatic mutations
- Acute myeloid leukemia with multilineage dysplasia
- Acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants
- Acute myeloid leukemia with t(8;21)(q22;q22) translocation
- Acute myelomonocytic leukemia
- Acute myelosclerosis
- Acute necrotizing encephalopathy of childhood
- Acute neonatal citrullinemia type 1
- Acute neonatal citrullinemia type I
- Acute neuronopathic Gaucher disease
- Acute non-herpetic encephalitis with severe refractory status epilepticus
- Acute non-lymphoblastic leukemia
- Acute opioid poisoning
- Acute panautonomic GBS
- Acute panautonomic Guillain-Barré syndrome
- Acute panautonomic neuropathy
- Acute pandysautonomia
- Acute panmyelosis with myelofibrosis
- Acute peripheral arterial occlusion
- Acute poisoning by drugs with membrane-stabilizing effect
- Acute promyelocytic leukemia
- Acute pure motor GBS
- Acute pure motor Guillain-Barré syndrome
- Acute pure sensory GBS
- Acute pure sensory Guillain-Barré syndrome
- Acute pure sensory neuropathy
- Acute rheumatic fever
- Acute sensorineural hearing loss by acute acoustic trauma or sudden deafness or surgery induced acoustic trauma
- Acute sensory ataxic GBS
- Acute sensory ataxic Guillain-Barré syndrome
- Acute sensory ataxic neuropathy
- Acute transverse myelitis
- Acute tricyclic antidepressant poisoning
- Acute tubulointerstitial nephritis and uveitis syndrome
- Acute undifferentiated leukemia
- Acute zonal occult outer retinopathy
- ACY1D
- ACY2 deficiency
- Acyl-CoA dehydrogenase 9 deficiency
- ACZ-responsive congenital myotonia
- ACZ-responsive myotonia
- Adactylia of hand, unilateral
- Adactyly of foot, bilateral
- Adactyly of foot, unilateral
- ADA deficiency
- Adair-Dighton syndrome
- Adamantinoma
- Adams-Oliver syndrome
- ADAM syndrome
- ADANE
- ADCA1
- ADCA3
- ADCA4
- ADCA-DN
- ADCAI
- ADCAIII
- ADCAIV
- ADCL
- ADCME
- AD-CNM
- Addison disease
- AD dRTA
- Adducted thumb-clubfoot syndrome
- Adducted thumbs - arthrogryposis, Christian type
- Adducted thumbs-arthrogryposis, Dundar type
- ADEAF
- ADEM
- Adenine phosphoribosyltransferase deficiency
- Adenocarcinoma of the cervix uteri
- Adenohypophysitis
- Adenoid basal carcinoma of the cervix uteri
- Adenoid cystic carcinoma of the cervix uteri
- Adenoid cystic carcinoma of the corpus uteri
- Adenomucinosis
- Adenosarcoma of the cervix uteri
- Adenosarcoma of the corpus uteri
- Adenosine deaminase deficiency
- Adenosine monophosphate deaminase deficiency
- Adenosylcobalamin deficiency
- Adenovirus infection in immunocompromised patients
- Adenylosuccinase deficiency
- Adenylosuccinate lyase deficiency
- AD-HED
- Adhesive arachnoiditis
- AD-HIES
- ADHR
- AD hypocalcemia
- Adiposalgia
- Adipose tissue rheumatism
- Adiposis dolorosa
- ADK hypermethioninemia
- ADLTE
- ADMERF
- ADNFLE
- ADNIV
- Adolescent benign focal crisis
- Adolescent idiopathic scoliosis
- ADOS
- ADPCLD
- ADPEAF
- adPEO
- ADP platelet receptor P2Y12 deficiency
- AD pRTA
- Adrenal crisis
- Adrenal incidentaloma
- Adrenal insufficiency - achalasia - alacrima
- Adrenocortical carcinoma
- Adrenocortical carcinoma with pure aldosterone hypersecretion
- Adrenocorticotropic hormone-independent macronodular adrenal hyperplasia
- Adrenocorticotropic hormone secretion syndrome
- Adrenomyeloneuropathy
- Adrenomyodystrophy
- ADSD
- ADSL deficiency
- Adult acute respiratory distress syndrome
- Adult ARDS
- Adult Bartter syndrome
- Adult basal ganglia disease
- Adult chronic recurrent multifocal osteomyelitis
- Adult CRMO
- Adult familial nephronophtisis - spastic quadriparesia
- Adult GM2 gangliosidosis 0 variant
- Adult heart tumor
- Adult hepatocellular carcinoma
- Adult hypophosphatasia
- Adult idiopathic neutropenia
- Adult intestinal botulism
- Adult intestinal colonization botulism
- Adult intestinal toxemia botulism
- Adult intestinal toxin-mediated botulism
- Adult Krabbe disease
- Adult NCL
- Adult neuronal ceroid lipofuscinosis
- Adult-onset Alpha-N-acetylgalactosaminidase deficiency
- Adult-onset autosomal dominant leukodystrophy
- Adult-onset autosomal recessive cerebellar ataxia
- Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
- Adult-onset citrin deficiency
- Adult-onset citrullinemia type 1
- Adult-onset citrullinemia type 2
- Adult-onset citrullinemia type I
- Adult-onset CPEO with mitochondrial myopathy
- Adult-onset dermatomyositis
- Adult-onset distal myopathy due to VCP mutation
- Adult-onset dystonia-parkinsonism
- Adult-onset focal torsion dystonia
- Adult-onset foveomacular vitelliform dystrophy
- Adult-onset GM1 gangliosidosis
- Adult-onset idiopathic torsion dystonia
- Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies
- Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
- Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency
- Adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency
- Adult-onset nemaline myopathy
- Adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia
- Adult-onset overlap myositis
- Adult-onset PLS
- Adult-onset polymyositis
- Adult-onset primary lateral sclerosis
- Adult-onset proximal spinal muscular atrophy, autosomal dominant
- Adult-onset SAPHO syndrome
- Adult-onset synovitis-acne-pustulosis-hyperostosis-osteitis syndrome
- Adult phosphoethanolaminuria
- Adult polyglucosan body disease
- Adult progeria
- Adult pulmonary Langerhans cell histiocytosis
- Adult pure red cell aplasia
- Adult Rathburn disease
- Adult Still's disease
- ADULT syndrome
- Adult T-cell leukemia/lymphoma
- ADVIRC
- Adynamia epidodica hereditaria
- AEC syndrome
- AEI
- AERRPS
- AFAP
- AFG3L2-associated spastic ataxia-neuropathy syndrome
- AFLP
- African iron overload
- African tick typhus
- African trypanosomiasis
- Agammaglobulinemia - microcephaly - craniosynostosis - severe dermatitis
- Agammaglobulinemia, non-Bruton type
- Aganglionic Megacolon
- Agenesis and aplasia of uterine body
- Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia
- Agenesis of the superior caval vein
- Agenesis of the superior vena cava
- Agenesis of the SVC
- AGEP
- Aggressive fibromatosis
- Aggressive NK-cell leukemia
- Aggressive NK-cell lymphoma
- Aggressive systemic mastocytosis
- Aglossia - adactylia
- Agnathia - holoprosencephaly - situs inversus
- Agnogenic myeloid metaplasia
- Agramatic variant of PPA
- Agramatic variant of primary progressive aphasia
- AHC
- AHDS
- Ahn-Lerman-Sagie syndrome
- AHO - PHP Ia
- AHO - PPHP
- aHUS
- Aicardi-Goutieres syndrome
- Aicardi syndrome
- AICA-ribosiduria
- AID deficiency
- AIDP
- AIDS wasting syndrome
- AIED
- AILT
- AIMAH
- AIP
- AIP type 1
- AIP type 2
- AIS
- AISA
- AK2 deficiency
- Akaba-Hayasaka syndrome
- AKE
- Akesson syndrome
- ALAD porphyria
- Alagille syndrome
- Alagille syndrome due to 20p12 microdeletion
- Alagille syndrome due to a JAG1 point mutation
- Alagille syndrome due to a NOTCH2 point mutation
- Alagille syndrome due to del(20)(p12)
- Alagille syndrome due to monosomy 20p12
- Alagille-Watson syndrome
- Alagille-Watson syndrome due to a JAG1 point mutation
- Alagille-Watson syndrome due to a NOTCH2 point mutation
- Alagille-Watson syndrome due to monosomy 20p12
- AL Amyloidosis
- Ĺland Island eye disease
- Alar cartilages hypoplasia - coloboma - telecanthus
- Al Awadi-Farag-Teebi syndrome
- Al-Awadi-Raas-Rothschild syndrome
- Albers-Schönberg osteopetrosis
- Albinism - black lock - cell migration disorder of the neurocytes of the gut - sensorineural deafness
- Albinism-deafness syndrome
- Albright hereditary osteodystrophy
- Albright hereditary osteodystrophy 3
- Albright hereditary osteodystrophy-like syndrome
- Albright hereditary osteodystrophy - PHP Ia
- Albright hereditary osteodystrophy - PPHP
- ALCL
- Alcohol antenatal infection
- Alcohol-responsive dystonia
- ALD
- ALDH18A1-related DeBarsy syndrome
- Aldosterone synthase deficiency
- Aldosterone synthase deficiency unlinked to CYP11B2
- Aldosterone synthase deficiency unlinked to the aldosterone synthase gene
- Aldred syndrome
- Alexander disease
- Alfi syndrome
- Al Frayh-Facharzt-Haque syndrome
- ALG11-CDG syndrome
- ALG12-CDG syndrome
- ALG13-CDG syndrome
- ALG1-CDG syndrome
- ALG2-CDG syndrome
- ALG3-CDG syndrome
- ALG6-CDG syndrome
- ALG8-CDG syndrome
- ALG9-CDG syndrome
- Al Gazali-Al Talabani syndrome
- Al Gazali-Aziz-Salem syndrome
- Al-Gazali-Dattani syndrome
- Al Gazali-Donnai-Muller syndrome
- al Gazali-Lytle syndrome
- Al Gazali-Nair syndrome
- Algodystrophy
- ALK+ ALCL
- ALK- ALCL
- ALK+ anaplastic large cell lymphoma
- ALK- anaplastic large cell lymphoma
- Alkaptonuria
- ALK-negative anaplastic large cell lymphoma
- ALK-positive anaplastic large cell lymphoma
- ALL
- Allain-Babin-Demarquez syndrome
- Allan-Herndon-Dudley syndrome
- Allergic aspergillosis
- Allergic bronchopulmonary aspergillosis
- Allgrove syndrome
- Alobar holoprosencephaly
- Alopecia - anosmia - deafness - hypogonadism
- Alopecia antibody deficiency
- Alopecia - contractures - dwarfism - intellectual deficit
- Alopecia - deafness - hypogonadism
- Alopecia-epilepsy-oligophrenia syndrome, Moynahan type
- Alopecia - epilepsy - pyorrhea - intellectual deficit
- Alopecia - epilepsy - pyorrhea - mental subnormality
- Alopecia - hypogonadism - extrapyramidal disorder
- Alopecia - intellectual deficit - hypergonadotropic hypogonadism
- Alopecia-intellectual deficit syndrome
- Alopecia - progressive neurological defect - endocrinopathy
- Alopecia totalis
- Alopecia universalis
- Alpers-Huttenlocher syndrome
- Alpers progressive sclerosing poliodystrophy
- Alpers syndrome
- Alpha-1,4-glucosidase acid deficiency
- Alpha-1,4-glucosidase acid deficiency, adult onset
- Alpha-1,4-glucosidase acid deficiency, infantile onset
- Alpha-1,4-glucosidase acid deficiency, juvenile onset
- Alpha-1-antichymotrypsin deficiency
- Alpha-1 antitrypsin deficiency
- Alpha-aminoadipic aciduria
- Alpha-B crystallin-related myofibrillar myopathy
- Alpha-crystallinopathy
- Alpha delta granule deficiency
- Alpha dense granule deficiency
- Alpha-galactosidase A deficiency
- Alpha-HCD
- Alpha heavy-chain disease
- Alpha-ketoglutarate dehydrogenase deficiency
- Alpha-L-fucosidase deficiency
- Alpha-L-iduronidase deficiency
- Alpha-mannosidosis
- Alpha-mannosidosis, adult form
- Alpha-mannosidosis, infantile form
- Alpha methyl acetoacetyl-CoA thiolase deficiency
- Alpha-methyl-acyl-CoA racemase deficiency
- Alpha-N-acetylgalactosaminidase deficiency
- Alpha-N-acetylgalactosaminidase deficiency type 1
- Alpha-N-acetylgalactosaminidase deficiency type 2
- Alpha-N-acetylgalactosaminidase deficiency type 3
- Alpha-sarcoglycanopathy
- Alpha storage pool deficiency
- Alpha-thalassemia
- Alpha-thalassemia hydrops fetalis
- Alpha thalassemia - intellectual deficit syndrome, deletion type
- Alpha thalassemia - intellectual deficit syndrome linked to chromosome 16
- Alpha-thalassemia intermedia
- Alpha-thalassemia major
- Alpha-thalassemia - myelodysplastic syndrome
- Alpha thalassemia - retardation syndrome
- Alpha thalassemia - retardation syndrome, X-linked
- Alpha thalassemia - X-linked intellectual deficit syndrome
- Alport deafness-nephropathy
- Alport syndrome
- Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis
- Alport syndrome with leukocyte inclusions and macrothrombocytopenia
- Alport syndrome with macrothrombocytopenia
- ALPS
- ALPS type 4
- ALPS type IV
- ALPS with recurrent infections
- ALS
- ALSG
- ALSP
- Alström syndrome
- ALT
- Alternating hemiplegia in childhood
- Alternating hemiplegia of childhood
- Alveolar capillary dysplasia with misalignment of pulmonary veins
- Alveolar capillary dysplasia with misalignment of pulmonary vessels
- Alveolar cleft lip and palate
- Alveolar echinococcosis
- Alveolar rhabdomyosarcoma
- Alveolar soft-part sarcoma
- Alveolar synechia - ankyloblepharon - ectodermal dysplasia
- Alves-dos Santos-Castelo syndrome
- ALX1-related frontonasal dysplasia
- ALX4-related FNDAG
- AMACR deficiency
- AMAN
- Amaurosis congenita of Leber
- Amaurosis - hypertrichosis
- Ambras syndrome
- Amelia of lower limb
- Amelia of lower limb, bilateral
- Amelia of lower limb, unilateral
- Amelia of upper limb
- Amelia of upper limb, bilateral
- Amelia of upper limb, unilateral
- Ameloblastic carcinoma
- Ameloblastoma
- Amelo-cerebro-hypohidrotic syndrome
- Amelogenesis imperfecta
- Amelogenesis imperfecta and gingival hyperplasia syndrome
- Amelogenesis imperfecta - nephrocalcinosis
- Amelogenesis imperfecta type 1
- Amelogenesis imperfecta type 2
- Amelogenesis imperfecta type 3
- Amelogenesis imperfecta type 4
- Amelo-onycho-hypohidrotic syndrome
- American mountain fever
- American trypanosomiasis
- Aminoaciduria, Hartnup type
- Aminoacylase 2 deficiency
- Aminopterin embryopathy syndrome
- Aminopterin/methotrexate embryofetopathy
- Aminopterin syndrome-like sine aminopterin
- Amish brittle hair syndrome
- Amish infantile epilepsy syndrome
- Amish lethal microcephaly
- Amish nemaline myopathy
- AMKL
- AML
- AML-M5
- AML-M6
- AML with CEBPA somatic mutations
- AMME complex
- AMME syndrome
- Amniotic bands
- Amniotic deformity - adhesion - mutilation syndrome
- aMOA
- Amoebiasis due to Entamoeba histolytica
- Amoebiasis due to free-living amoebae
- AMP deaminase deficiency
- Ampola syndrome
- Ampulla cardiomyopathy
- Ampullary carcinoma
- Ampulloma
- AMSAN
- Amylo-1,6-glucosidase deficiency
- Amyloid lichen
- Amyloidosis AA
- Amyloidosis cutis dyschromia
- Amyloidosis cutis dyschromica
- Amyloidosis, Ostertag type
- Amylopectinosis
- Amyoplasia congenita
- Amyotrophic lateral sclerosis
- Amyotrophic lateral sclerosis, hemiplegic type
- Amyotrophic lateral sclerosis-parkinsonism-dementia complex
- Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam
- Amyotrophy - fat tissue anomaly
- Anal endocrine tumor
- Anal fistula
- Anaphylactoid purpura
- Anaplastic astrocytoma
- Anaplastic ependymoma
- Anaplastic ganglioglioma
- Anaplastic large cell lymphoma
- Anaplastic/large cell medulloblastoma
- Anaplastic oligoastrocytoma
- Anaplastic oligodendroglioma
- Anaplastic thyroid carcinoma
- Anauxetic dysplasia
- ANCL
- Ancylostomiasis
- Andermann syndrome
- Andersen cardiodysrhythmic periodic paralysis
- Andersen disease
- Andersen syndrome
- Andersen-Tawil syndrome
- Anderson disease
- Anderson-Fabry disease
- Androblastoma
- Androgenetic/biparental mosaicism
- Androgen insensitivity syndrome
- Androgen resistance syndrome
- ANEC
- Anemia due to adenosine triphosphatase deficiency
- ANE syndrome
- Aneurysmal telangiectasia
- Aneurysm of sinus of Valsalva
- Aneurysm or dilatation of ascending aorta
- Aneurysm - osteoarthritis syndrome
- Angelman syndrome
- Angelman syndrome due to maternal 15q11q13 deletion
- Angelman syndrome due to maternal monosomy 15q11q13
- Angelman syndrome due to paternal uniparental disomy of chromosome 15
- Angel-shaped phalango-epiphyseal dysplasia
- Angiocentric glioma
- Angiocentric T-cell lymphoma
- Angiodysgenetic necrotizing myelopathy
- Angioendotheliomatosis proliferans systemisata
- Angiofollicular ganglionic hyperplasia
- Angiofollicular lymph hyperplasia
- Angioimmunoblastic T-cell lymphoma
- Angiokeratoma Corporis Diffusum
- Angioma serpiginosum
- Angio-osteohypertrophic syndrome
- Angio-osteohypotrophic syndrome
- Angiosarcoma
- Angiostrongyliasis
- Angiotropic large cell lymphoma
- Anguilluliasis
- Anguillulosis
- Anhidrotic ectodermal dysplasia
- Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
- Anhidrotic ectodermal dysplasia with immunodeficiency
- Anhidrotic ectodermic dysplasia - cleft lip/palate
- Aniridia
- Aniridia - absent patella
- Aniridia - cerebellar ataxia - intellectual deficit
- Aniridia-intellectual deficit syndrome
- Aniridia - ptosis - intellectual deficit - familial obesity
- Aniridia - renal agenesis - psychomotor retardation
- Anisakiasis
- Ankyloblepharon - ectodermal defects - cleft lip/palate
- Ankyloblepharon filiforme adnatum - cleft palate
- Ankyloblepharon filiforme - imperforate anus
- Ankylosing vertebral hyperostosis with tylosis
- Ankylosis of teeth
- Ankylostomiasis
- Annular atrophic lichen planus
- Annular atrophic LP
- Annular epidermolytic ichthyosis
- Annular lichen planus
- Annular LP
- Annular pancreas
- Annuloaortic ectasia
- Anodontia
- Anomaly of the mitral subvalvular apparatus
- Anomaly of the tricuspid subvalvular apparatus
- Anomaly of the tricuspid valve chordae
- Anonychia
- Anonychia congenita totalis
- Anonychia - microcephaly
- Anonychia - onychodystrophy
- Anonychia - onychodystrophy with hypoplasia or absence of distal phalanges
- Anonychia with flexural pigmentation
- Anophthalmia - esophageal-genital syndrome
- Anophthalmia - heart and pulmonary anomalies - intellectual deficit
- Anophthalmia - hypothalamo-pituitary insufficiency
- Anophthalmia - megalocornea - cardiopathy - skeletal anomalies
- Anophthalmia/microphthalmia - esophageal atresia
- Anophthalmia plus syndrome
- Anophthalmia - pulmonary hypoplasia
- Anophthalmia - syndactyly
- ANOTHER syndrome
- Anotia
- Antecubital pterygium syndrome
- Antenatal Bartter syndrome
- Antenatal Epstein-Barr virus infection
- Antenatal multiminicore disease with arthrogryposis multiplex congenita
- Anterior encephalocele
- Anterior limiting membrane dystrophy type I
- Anterior limiting membrane dystrophy type II
- Anterior pituitary hypophysitis
- Anterior polar cataract
- Anterior subcapsular cataract
- Anthracycline extravasations
- Anti-glomerular basement membrane antibody-mediated disease
- Anti-HLA hyperimmunization
- Antinolo-Nieto-Borrego syndrome
- Anti-SRP myopathy
- Antisynthetase syndrome
- Antley-Bixler-like syndrome - ambiguous genitalia - disordered steroidogenesis
- Antley-Bixler syndrome
- Antley-Bixler syndrome, POR-related
- Antley-Bixler syndrome type 2
- Antley-Bixler syndrome with genital anomaly and disorder of steroidogenesis
- AOA1
- AOA2
- AOI
- Aorta coarctation
- Aorta-pulmonary artery fistula
- Aortic aneurysm syndrome due to TGF-beta receptors anomalies
- Aortic arch anomaly - peculiar facies - intellectual deficit
- Aortic arch defects
- Aortic arch interruption
- Aortic dilatation - joint hypermobility - arterial tortuosity
- Aortic valve atresia
- Aortic valve dysplasia
- Aorto-left ventricular tunnel
- Aorto-pulmonary coronary arterial course
- Aorto-right ventricular tunnel
- Aorto-ventricular tunnel
- AOS
- AOS
- AP4 deficiency syndrome
- APBD
- APC-related AFAP
- APC-related attenuated familial adenomatous polyposis
- APC-related attenuated familial polyposis coli
- APC-related attenuated FAP
- APECED syndrome
- Apert syndrome
- Apertura pyriformis with holoprosencephaly
- Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis
- Aphalangy - syndactyly - microcephaly
- Aphallia
- Aphonia - deafness - retinal dystrophy - bifid halluces - intellectual deficit
- Aphonia - deafness - retinal dystrophy - duplicated halluces - intellectual deficit
- Apical ballooning syndrome
- aPLAID
- Aplasia cutis congenita - epibulbar dermoids
- Aplasia cutis congenita - intestinal lymphangiectasia
- Aplasia Cutis Congenita Verticis
- Aplasia cutis - myopia
- Aplasia/hypoplasia of limbs and pelvis
- Aplasia of lacrimal and salivary glands
- Aplasia of tibia with split-hand/split-foot deformity
- Apnea of infancy
- Apnea of prematurity
- ApoC-II deficiency
- Apodia
- Apodia, bilateral
- Apodia, unilateral
- Apolipoprotein AI amyloidosis
- Apolipoprotein A-I deficiency
- Apolipoprotein AII amyloidosis
- Apparent mineralocorticoid excess
- Appendiceal endocrine tumor
- Apple peel syndrome
- Aprosencephaly cerebellar dysgenesis
- APRT deficiency
- APS1
- APS2
- APS3
- APS4
- APS type 2
- APS type 3
- APS type 4
- APV/ADA, Fallot type
- APV/PDA, non Fallot-type
- Arachnodactyly - abnormal ossification - intellectual deficit
- Arachnodactyly - intellectual deficit - dysmorphism
- Arachnoid cyst
- Arachnoiditis
- ARAN-NM
- Arbovirus fever
- ARCA1
- ARCA2
- ARCL1
- ARCL2
- AR-CMT1
- AR-CMT2
- AR-CMT2B1
- AR-CMT2B2
- AR-CMT2C
- ARCMT2K
- ARCMT2-NM
- AR-CNM
- ARC syndrome
- AR dRTA with hearing loss
- AR dRTA without deafness
- AR dRTA without hearing loss
- AR dRTA wth deafness
- AREDYLD syndrome
- Areflexic dystasia, hereditary, Roussy-Levy type
- Aregenerative anemia
- Arena syndrome
- Areolar atrophy of the macula
- Argentine hemorrhagic fever
- Argentinian hemorrhagic fever
- Arginase deficiency
- Arginine:glycine amidinotransferase deficiency
- Argininemia
- Argininosuccinase deficiency
- Argininosuccinate synthase deficiency
- Argininosuccinate synthetase deficiency
- Argininosuccinic acid synthase deficiency
- Argininosuccinic acid synthetase deficiency
- Argininosuccinic aciduria
- Argyria
- Argyrophilic grain disease
- AR-HED
- AR-HIES
- AR-HIES due to TYK2 deficiency
- ARHR
- AR-hyper IgE syndrome due to TYK2 deficiency
- Arias syndrome
- Arima syndrome
- Arkless-Graham syndrome
- Armfield syndrome
- Arndt-Gottron disease
- Arnold-Chiari malformation type 1
- Arnold-Chiari malformation type 2
- Arnold-Chiari malformation type I
- Arnold-Chiari malformation type II
- Aromatase deficiency
- Aromatase excess syndrome
- Aromatic L-amino acid decarboxylase deficiency
- arPEO
- AR pRTA
- Arrhenoblastoma
- Arrhinia
- Arrhinia - choanal atresia - microphthalmia
- Arrhythmogenic right ventricular cardiomyopathy
- Arrhythmogenic right ventricular dysplasia
- ARSACS
- ARSAL
- ARSB deficiency
- Arterial dissection - lentiginosis
- Arterial tortuosity syndrome
- Arteriohepatic dysplasia
- Arteriohepatic dysplasia due to a JAG1 point mutation
- Arteriohepatic dysplasia due to a NOTCH2 point mutation
- Arteriohepatic dysplasia due to monosomy 20p12
- Arthritis urethritica
- Arthrogryposis due to muscular dystrophy
- Arthrogryposis - ectodermal dysplasia - other anomalies
- Arthrogryposis - epileptic seizures - migrational brain disorder
- Arthrogryposis - hyperkeratosis, lethal form
- Arthrogryposis-like hand anomaly - sensorineural deafness
- Arthrogryposis-like syndrome
- Arthrogryposis multiplex congenita
- Arthrogryposis multiplex congenita - pulmonary hypoplasia
- Arthrogryposis multiplex congenita - whistling face
- Arthrogryposis - renal dysfunction - cholestasis
- Arthrogryposis - severe scoliosis
- Arthrogryposis with oculomotor limitation and electroretinal anomalies
- Arthropathy-camptodactyly syndrome
- Arts syndrome
- ARVC
- ARVD
- Arylsulfatase A deficiency
- Arylsulfatase A deficiency, adult form
- Arylsulfatase A deficiency, juvenile form
- Arylsulfatase A deficiency, late infantile form
- Arylsulfatase B deficiency
- ASAN
- ASB deficiency
- Asbestos intoxication
- Asbestosis
- Ascher syndrome
- ASD
- ASD, coronary sinus type
- ASD due to AUTS2 deficiency
- ASD, ostium primum type
- ASD, ostium secundum type
- ASD, sinus venosus type
- Aseptic abscesses syndrome
- Aseptic necrosis of patella
- Aseptic necrosis of phalangeal epiphyses
- Aseptic necrosis of the capital femoral epiphysis
- Aseptic necrosis of the capital humerus
- Aseptic necrosis of the lunate bone
- Aseptic necrosis of the tarsal bone
- Aseptic necrosis of the tibial tubercle
- Aseptic osteitis
- Aseptic systemic abscesses
- Asherman's syndrome
- Aspartoacylase deficiency
- Aspartylglucosaminidase deficiency
- Aspartylglucosaminuria
- ASPED
- Aspergillosis
- Asphyxiating thoracic dystrophy of the newborn
- ASSA
- ASS deficiency
- Astley-Kendall dysplasia
- Astroblastoma
- Astrocytic tumor
- Astrocytoma
- Ataxia-deafness-retardation syndrome
- Ataxia - delayed dentition - hypomyelination
- Ataxia - diabetes - goiter - gonadal insufficiency
- Ataxia - hypogonadism - choroidal dystrophy
- Ataxia - oculomotor apraxia type 1
- Ataxia - oculomotor apraxia type 2
- Ataxia - pancytopenia
- Ataxia - photosensitivity - short stature
- Ataxia - tapetoretinal degeneration
- Ataxia-telangiectasia
- Ataxia-telangiectasia-like disorder
- Ataxia-telangiectasia, variant 1
- Ataxia with isolated vitamin E deficiency
- Ataxia with vitamin E deficiency
- Ataxo-opso-myoclonus syndrome
- ATCS
- Atelencephaly
- Atelosteogenesis I
- Atelosteogenesis type II
- Atelosteogenesis type III
- Athabaskan brainstem dysgenesis syndrome
- Atherosclerosis- deafness - diabetes - epilepsy - nephropathy
- Athyreosis
- ATIC deficiency
- Atkin-Flaitz syndrome
- Atlantoaxial subluxation
- ATLD
- ATLL
- ATMDS
- ATM/TM
- Atopic keratoconjunctivitis
- ATR-16 syndrome
- Atresia of bile ducts
- Atresia of small intestine
- Atresia of urethra
- Atrial cardiomyopathy with heart block
- Atrial septal aneurysm
- Atrial septal defect
- Atrial septal defect - atrioventricular conduction defects
- Atrial septal defect, coronary sinus type
- Atrial septal defect, ostium primum type
- Atrial septal defect, ostium secundum type
- Atrial septal defect, sinus venosus type
- Atrial stand still
- Atrial tachyarrhythmia with short PR interval
- Atrichia - mental and growth delay
- Atrichia with papular lesions
- Atrio-digital dysplasia, Slovenian type
- Atriodigital dysplasia type 1
- Atriodigital dysplasia type 2
- Atriodigital dysplasia type 3
- Atrioventricular defect - blepharophimosis -radial defects
- Atrophia areata
- Atrophia bulborum hereditaria
- Atrophic lichen planus
- Atrophic LP
- Atrophoderma vermiculata
- ATR syndrome, deletion type
- ATR syndrome linked to chromosome 16
- AT/RT
- ATRUS syndrome
- ATR-X syndrome
- ATS
- ATS-MR
- Attenuated Chédiak-Higashi syndrome
- Attenuated familial adenomatous polyposis
- Attenuated familial polyposis coli
- Attenuated FAP
- ATTR cardiomyopathy
- AT V1
- Atypical arterial duct
- Atypical autism
- Atypical Chédiak-Higashi syndrome
- Atypical chronic myeloid leukemia
- Atypical coarctation of aorta
- Atypical Demons-Meigs syndrome
- Atypical dentin dysplasia due to SMOC2 deficiency
- Atypical Gaucher disease due to saposin C deficiency
- Atypical glycine encephalopathy
- Atypical granular corneal dystrophy
- Atypical HCS
- Atypical hemolytic uremic syndrome
- Atypical hemolytic uremic syndrome with antibody anti-factor H
- Atypical hemolytic uremic syndrome with B factor anomaly
- Atypical hemolytic uremic syndrome with C3 anomaly
- Atypical hemolytic uremic syndrome with H factor anomaly
- Atypical hemolytic uremic syndrome with I factor anomaly
- Atypical hemolytic uremic syndrome with MCP/CD46 anomaly
- Atypical hemolytic uremic syndrome with thrombomodulin anomaly
- Atypical HUS
- Atypical hypotonia - cystinuria syndrome
- Atypical lichen myxedematosus
- Atypical lipoma
- Atypical lipomatous tumor
- Atypical Mayer-Rokitansky-Küster-Hauser syndrome
- Atypical Meigs syndrome
- Atypical MRKH syndrome
- Atypical Norrie disease due to del(X)(p11.3)
- Atypical Norrie disease due to monosomy Xp11.3
- Atypical Norrie disease due to Xp11.3 microdeletion
- Atypical pantothenate kinase associated neurodegeneration
- Atypical papilloma of choroid plexus
- Atypical patent ductus arteriosus
- Atypical progeroid syndrome
- Atypical progressive supranuclear palsy
- Atypical PSP
- Atypical Rett syndrome
- Atypical Rokitansky syndrome
- Atypical RTT
- Atypical teratoid/rhabdoid tumor
- Atypical teratoid tumor
- Atypical tuberous myxedema of Jadassohn-Dosseker
- Atypical Werner syndrome
- Atypical X-linked achromatopsia
- Aughton-Hufnagle syndrome
- Aural atresia - multiple congenital anomalies - intellectual deficit
- Auralcephalosyndactyly
- Auricular abnormalities - cleft lip with or without cleft palate - ocular abnormalities
- Auriculo-condylar syndrome
- Auriculoocular anomalies - cleft lip
- Auriculoosteodysplasia
- Aurocephalosyndactyly
- Ausems-Wittebol Post-Hennekam syndrome
- Austin type juvenile sulfatidosis
- Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
- Autism - facial port-wine stain
- Autism spectrum disorder due to AUTS2 deficiency
- Autoerythrocyte sensitization syndrome
- Autoimmune Addison's disease
- Autoimmune adrenalitis
- Autoimmune enteropathy
- Autoimmune enteropathy type 1
- Autoimmune enteropathy type 2
- Autoimmune enteropathy type 3
- Autoimmune hemolytic anemia, warm type
- Autoimmune hepatitis
- Autoimmune hypoparathyroidism
- Autoimmune hypoparathyroidism - chronic candidiasis - Addison's disease
- Autoimmune hypoparathyroidism - chronic candidosis - Addison's disease
- Autoimmune lymphoproliferative syndrome
- Autoimmune lymphoproliferative syndrome type 4
- Autoimmune lymphoproliferative syndrome type IV
- Autoimmune lymphoproliferative syndrome with recurrent infections
- Autoimmune myasthenia gravis
- Autoimmune necrotizing myopathy
- Autoimmune pancreatitis
- Autoimmune pancreatitis type 1
- Autoimmune pancreatitis type 2
- Autoimmune PAP
- Autoimmune polyendocrine syndrome type 1
- Autoimmune polyendocrine syndrome type 2
- Autoimmune polyendocrine syndrome type 3
- Autoimmune polyendocrine syndrome type 4
- Autoimmune polyendocrinopathy - candidiasis - ectodermal dystrophy syndrome
- Autoimmune polyendocrinopathy - candidosis - ectodermal dystrophy syndrome
- Autoimmune polyendocrinopathy type 1
- Autoimmune polyendocrinopathy type 2
- Autoimmune polyendocrinopathy type 3
- Autoimmune polyendocrinopathy type 4
- Autoimmune polyglandular syndrome type 1
- Autoimmune polyglandular syndrome type 2
- Autoimmune polyglandular syndrome type 3
- Autoimmune polyglandular syndrome type 4
- Autoimmune pulmonary alveolar proteinosis
- Autoimmune thrombocytopenia
- Autoimmune thyroid disease and/or type 1 diabetes - Addison's disease
- Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
- Autoinflammatory disease due to interleukin-1 receptor antagonist deficiency
- Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
- Autosmal recessive spastic ataxia of Charlevoix-Saguenay
- Autosomal agammaglobulinemia
- Autosomal codominant severe lipodystrophic laminopathy
- Autosomal dominant Alport syndrome
- Autosomal dominant anhidrotic ectodermal dysplasia
- Autosomal dominant aplasia and myelodysplasia
- Autosomal dominant aplastic anemia and myelodysplasia
- Autosomal dominant axonal Charcot-Marie-Tooth disease
- Autosomal dominant BECRS
- Autosomal dominant benign distal spinal muscular atrophy
- Autosomal dominant beta2-microglobulinic amyloidosis
- Autosomal dominant brachyolmia
- Autosomal dominant centronuclear myopathy
- Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome
- Autosomal dominant cerebellar ataxia type 1
- Autosomal dominant cerebellar ataxia type 3
- Autosomal dominant cerebellar ataxia type 4
- Autosomal dominant cerebellar ataxia type I
- Autosomal dominant cerebellar ataxia type III
- Autosomal dominant cerebellar ataxia type IV
- Autosomal dominant Charcot-Marie-Tooth disease type 2
- Autosomal dominant Charcot-Marie-Tooth disease type 2A1
- Autosomal dominant Charcot-Marie-Tooth disease type 2A2
- Autosomal dominant Charcot-Marie-Tooth disease type 2B
- Autosomal dominant Charcot-Marie-Tooth disease type 2C
- Autosomal dominant Charcot-Marie-Tooth disease type 2D
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
- Autosomal dominant Charcot-Marie-Tooth disease type 2E
- Autosomal dominant Charcot-Marie-Tooth disease type 2F
- Autosomal dominant Charcot-Marie-Tooth disease type 2G
- Autosomal dominant Charcot-Marie-Tooth disease type 2I
- Autosomal dominant Charcot-Marie-Tooth disease type 2J
- Autosomal dominant Charcot-Marie-Tooth disease type 2K
- Autosomal dominant Charcot-Marie-Tooth disease type 2L
- Autosomal dominant Charcot-Marie-Tooth disease type 2M
- Autosomal dominant Charcot-Marie-Tooth disease type 2N
- Autosomal dominant Charcot-Marie-Tooth disease type 2O
- Autosomal dominant Charcot-Marie-Tooth disease type 2P
- Autosomal dominant Charcot-Marie-Tooth disease type 2Q
- Autosomal dominant CHED
- Autosomal dominant childhood-onset cortical cataract
- Autosomal dominant childhood-onset progressive cortical cataract
- Autosomal dominant chorioretinopathy - microcephaly
- Autosomal dominant coarctation of aorta
- Autosomal dominant congenital benign spinal muscular atrophy
- Autosomal dominant congenital hereditary endothelial dystrophy
- Autosomal dominant cortical myoclonus and epilepsy
- Autosomal dominant cutis laxa
- Autosomal dominant cystoid macular edema
- Autosomal dominant demyelinating Charcot-Marie-Tooth disease
- Autosomal dominant diffuse palmoplantar keratoderma, Norrbotten type
- Autosomal dominant distal juvenile spinal muscular atrophy type 1
- Autosomal dominant distal renal tubular acidosis
- Autosomal dominant dopa-responsive dystonia
- Autosomal dominant dystrophic epidermolysis bullosa, Cockayne-Touraine type
- Autosomal dominant dystrophic epidermolysis bullosa, Pasini and Cockayne-Touraine types
- Autosomal dominant dystrophic epidermolysis bullosa, Pasini type
- Autosomal dominant ectodermal dysplasia-cancer predisposition syndrome syndrome
- Autosomal dominant Emery-Dreifuss muscular dystrophy
- Autosomal dominant epilepsy with auditory features
- Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
- Autosomal dominant familial spastic paraplegia type 3
- Autosomal dominant focal dystonia, DYT25
- Autosomal dominant focal dystonia, DYT7 type
- Autosomal dominant gingival fibromatosis
- Autosomal dominant gingival hyperplasia
- Autosomal dominant hereditary hemochromatosis
- Autosomal dominant HIES
- Autosomal dominant hyper IgE syndrome
- Autosomal dominant hyperimmunoglobulin E syndrome
- Autosomal dominant hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
- Autosomal dominant hyperinsulinemic hypoglycemia due to SUR1 deficiency
- Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
- Autosomal dominant hyperinsulinism due to SUR1 deficiency
- Autosomal dominant hypocalcemia
- Autosomal dominant hypohidrotic ectodermal dysplasia
- Autosomal dominant hypophosphatemia
- Autosomal dominant hypophosphatemic rickets
- Autosomal dominant intermediate Charcot-Marie-Tooth disease
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
- Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
- Autosomal dominant isolated neurosensory deafness type DFNA
- Autosomal dominant isolated neurosensory hearing loss type DFNA
- Autosomal dominant isolated sensorineural deafness type DFNA
- Autosomal dominant isolated sensorineural hearing loss type DFNA
- Autosomal dominant Kenny-Caffey syndrome
- Autosomal dominant keratitis
- Autosomal dominant keratoconus with early-onset anterior polar cataracts
- Autosomal dominant Larsen syndrome
- Autosomal dominant late-onset retinal degeneration
- Autosomal dominant lateral temporal lobe epilepsy
- Autosomal dominant leukoencephalopathy with neuroaxonal spheroids
- Autosomal dominant limb-girdle muscular dystrophy type 1A
- Autosomal dominant limb-girdle muscular dystrophy type 1B
- Autosomal dominant limb-girdle muscular dystrophy type 1C
- Autosomal dominant limb-girdle muscular dystrophy type 1D
- Autosomal dominant limb-girdle muscular dystrophy type 1E
- Autosomal dominant limb-girdle muscular dystrophy type 1F
- Autosomal dominant limb-girdle muscular dystrophy type 1G
- Autosomal dominant limb-girdle muscular dystrophy type 1H
- Autosomal dominant macrothrombocytopenia
- Autosomal dominant medullary cystic kidney disease with hyperuricemia
- Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
- Autosomal dominant medullary cystic kidney disease without hyperuricemia
- Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
- Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
- Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency
- Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency
- Autosomal dominant methemoglobinemia
- Autosomal dominant microcephaly
- Autosomal dominant MSMD due to partial IFNgammaR1 deficiency
- Autosomal dominant MSMD due to partial IFNgammaR2 deficiency
- Autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency
- Autosomal dominant MSMD due to partial interferon gamma receptor 2 deficiency
- Autosomal dominant multiple pterygium syndrome
- Autosomal dominant myoglobinuria
- Autosomal dominant nail dysplasia
- Autosomal dominant neovascular inflammatory vitreoretinopathy
- Autosomal dominant nephronophthisis
- Autosomal dominant nocturnal frontal lobe epilepsy
- Autosomal dominant nonsyndromic intellectual deficit
- Autosomal dominant nonsyndromic neurosensory deafness type DFNA
- Autosomal dominant nonsyndromic neurosensory hearing loss type DFNA
- Autosomal dominant nonsyndromic sensorineural deafness type DFNA
- Autosomal dominant nonsyndromic sensorineural hearing loss type DFNA
- Autosomal dominant omodysplasia
- Autosomal dominant Opitz BBB/G syndrome
- Autosomal dominant Opitz G/BBB syndrome
- Autosomal dominant Opitz syndrome
- Autosomal dominant optic atrophy and cataract
- Autosomal dominant optic atrophy and congenital deafness
- Autosomal dominant optic atrophy and late-onset deafness
- Autosomal dominant optic atrophy and peripheral neuropathy
- Autosomal dominant optic atrophy, classic type
- Autosomal dominant optic atrophy, Kjer type
- Autosomal dominant optic atrophy plus syndrome
- Autosomal dominant optic atrophy type 3
- Autosomal dominant osteopetrosis type 1
- Autosomal dominant osteosclerosis, Stanescu type
- Autosomal dominant osteosclerosis, Worth type
- Autosomal dominant palmoplantar hyperkeratosis and congenital alopecia
- Autosomal dominant palmoplantar keratoderma and congenital alopecia
- Autosomal dominant periodic fever
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
- Autosomal dominant polycystic liver disease
- Autosomal dominant popliteal pterygium syndrome
- Autosomal dominant primary hypomagnesemia with hypocalcuria
- Autosomal dominant prognathism
- Autosomal dominant progressive external ophthalmoplegia
- Autosomal dominant progressive nephropathy with hypertension
- Autosomal dominant proximal renal tubular acidosis
- Autosomal dominant pseudohypoaldosteronism type 1
- Autosomal dominant rhegmatogenous retinal detachment
- Autosomal dominant Robinow syndrome
- Autosomal dominant secondary erythrocytosis
- Autosomal dominant secondary polycythemia
- Autosomal dominant Segawa syndrome
- Autosomal dominant severe congenital neutropenia
- Autosomal dominant slowed nerve conduction velocity
- Autosomal dominant spastic ataxia 1
- Autosomal dominant spastic paraplegia type 10
- Autosomal dominant spastic paraplegia type 12
- Autosomal dominant spastic paraplegia type 13
- Autosomal dominant spastic paraplegia type 17
- Autosomal dominant spastic paraplegia type 19
- Autosomal dominant spastic paraplegia type 29
- Autosomal dominant spastic paraplegia type 3
- Autosomal dominant spastic paraplegia type 31
- Autosomal dominant spastic paraplegia type 36
- Autosomal dominant spastic paraplegia type 37
- Autosomal dominant spastic paraplegia type 38
- Autosomal dominant spastic paraplegia type 4
- Autosomal dominant spastic paraplegia type 41
- Autosomal dominant spastic paraplegia type 42
- Autosomal dominant spastic paraplegia type 6
- Autosomal dominant spastic paraplegia type 8
- Autosomal dominant spastic paraplegia type 9
- Autosomal dominant spinocerebellar ataxia type 7
- Autosomal dominant spondylocostal dysostosis
- Autosomal dominant spondylocostal dysplasia
- Autosomal dominant striatal neurodegeneration
- Autosomal dominant striatonigral degeneration
- Autosomal dominant vitreoretinochoroidopathy
- Autosomal recessive acrofacial dysostosis
- Autosomal recessive Alport syndrome
- Autosomal recessive amelia
- Autosomal recessive anhidrotic ectodermal dysplasia
- Autosomal recessive aplasia cutis
- Autosomal recessive ataxia, Beauce type
- Autosomal recessive ataxia due to coenzyme Q10 deficiency
- Autosomal recessive ataxia due to PEX10 deficiency
- Autosomal recessive ataxia due to ubiquinone deficiency
- Autosomal recessive axonal Charcot-Marie-Tooth disease type 2
- Autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2
- Autosomal recessive axonal Charcot-Marie-Tooth disease type 2K
- Autosomal recessive axonal Charcot-Marie-Tooth disease type 4C
- Autosomal recessive axonal CMT4C1
- Autosomal recessive axonal CMT4C2
- Autosomal recessive axonal CMT4C3
- Autosomal recessive axonal CMT4C4
- Autosomal recessive axonal neuropathy with neuromyotonia
- Autosomal recessive bestrophinopathy
- Autosomal recessive carpotarsal osteolysis
- Autosomal recessive centronuclear myopathy
- Autosomal recessive cerebellar ataxia - blindness - deafness
- Autosomal recessive cerebellar ataxia - cognitive defect
- Autosomal recessive cerebellar ataxia due to GBA2 deficiency
- Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
- Autosomal recessive cerebellar ataxia - psychomotor retardation
- Autosomal recessive cerebellar ataxia - saccadic intrusion
- Autosomal recessive cerebellar ataxia type 1
- Autosomal recessive cerebellar ataxia with late-onset spasticity
- Autosomal recessive cerebelloparenchymal disorder type 3
- Autosomal recessive Charcot-Marie-Tooth disease, Ouvrier type
- Autosomal recessive Charcot-Marie-Tooth disease type 2B1
- Autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia
- Autosomal recessive Charcot-Marie-Tooth disease with hoarseness
- Autosomal recessive CHED
- Autosomal recessive childhood-onset cortical cataract
- Autosomal recessive chorioretinopathy - microcephaly
- Autosomal recessive complex HSP
- Autosomal recessive complex spastic paraplegia
- Autosomal recessive complex SPG
- Autosomal recessive complicated HSP
- Autosomal recessive complicated spastic paraplegia
- Autosomal recessive complicated SPG
- Autosomal recessive congenital cerebellar ataxia due to metabotropic glutamate receptor 1 deficiency
- Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency
- Autosomal recessive congenital hereditary endothelial dystrophy
- Autosomal recessive congenital hypomyelinating neuropathy
- Autosomal recessive congenital sideroblastic anemia
- Autosomal recessive cutis laxa, Debré type
- Autosomal recessive cutis laxa, pulmonary emphysema type
- Autosomal recessive cutis laxa type 1
- Autosomal recessive cutis laxa type 2
- Autosomal recessive cutis laxa with severe systemic involvement
- Autosomal recessive deafness-onychodystrophy syndrome
- Autosomal recessive demyelinating Charcot-Marie-Tooth
- Autosomal recessive distal osteolysis syndrome
- Autosomal recessive distal renal tubular acidosis with deafness
- Autosomal recessive distal renal tubular acidosis with hearing loss
- Autosomal recessive distal renal tubular acidosis without deafness
- Autosomal recessive distal renal tubular acidosis without hearing loss
- Autosomal recessive distal spinal muscular atrophy type 1
- Autosomal recessive distal spinal muscular atrophy type 2
- Autosomal recessive distal spinal muscular atrophy type 3
- Autosomal recessive distal spinal muscular atrophy type 4
- Autosomal recessive distal spinal muscular atrophy type 5
- Autosomal recessive dopa-responsive dystonia
- Autosomal recessive dystrophic epidermolysis bullosa generalisata gravis
- Autosomal recessive dystrophic epidermolysis bullosa generalisata mitis
- Autosomal recessive dystrophic epidermolysis bullosa, generalized other
- Autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type
- Autosomal recessive early-onset IBD
- Autosomal recessive early-onset inflammatory bowel disease
- Autosomal recessive Emery-Dreifuss muscular dystrophy
- Autosomal recessive epidermolysis bullosa simplex
- Autosomal recessive exfoliative ichthyosis
- Autosomal recessive facio-digito-genital syndrome
- Autosomal recessive frontotemporal pachygyria
- Autosomal recessive HIES
- Autosomal recessive hyper IgE syndrome
- Autosomal recessive hyper IgE syndrome due to TYK2 deficiency
- Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
- Autosomal recessive hyperinsulinemic hypoglycemia due to SUR1 deficiency
- Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
- Autosomal recessive hyperinsulinism due to SUR1 deficiency
- Autosomal recessive hypohidrotic ectodermal dysplasia
- Autosomal recessive hypophosphatemic rickets
- Autosomal recessive infantile hypercalcemia
- Autosomal recessive intellectual deficit due to TRAPPC9 deficiency
- Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
- Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
- Autosomal recessive intermediate osteopetrosis
- Autosomal recessive isolated neurosensory deafness type DFNB
- Autosomal recessive isolated sensorineural deafness type DFNB
- Autosomal recessive Kenny-Caffey syndrome
- Autosomal recessive Larsen syndrome
- Autosomal recessive lethal multiple pterygium syndrome
- Autosomal recessive leukoencephalopathy with ischemic stroke-retinitis pigmentosa syndrome
- Autosomal recessive LGMD due to ISPD deficiency
- Autosomal recessive LGMD with cerebellar involvement
- Autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency
- Autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency
- Autosomal recessive limb-girdle muscular dystrophy - dystroglycanopathy type C7
- Autosomal recessive limb girdle muscular dystrophy type 2A
- Autosomal recessive limb-girdle muscular dystrophy type 2B
- Autosomal recessive limb-girdle muscular dystrophy type 2C
- Autosomal recessive limb-girdle muscular dystrophy type 2D
- Autosomal recessive limb-girdle muscular dystrophy type 2E
- Autosomal recessive limb-girdle muscular dystrophy type 2F
- Autosomal recessive limb-girdle muscular dystrophy type 2G
- Autosomal recessive limb-girdle muscular dystrophy type 2H
- Autosomal recessive limb-girdle muscular dystrophy type 2I
- Autosomal recessive limb-girdle muscular dystrophy type 2J
- Autosomal recessive limb-girdle muscular dystrophy type 2K
- Autosomal recessive limb-girdle muscular dystrophy type 2L
- Autosomal recessive limb-girdle muscular dystrophy type 2M
- Autosomal recessive limb-girdle muscular dystrophy type 2N
- Autosomal recessive limb-girdle muscular dystrophy type 2O
- Autosomal recessive limb-girdle muscular dystrophy type 2Q
- Autosomal recessive limb-girdle muscular dystrophy with cerebellar involvement
- Autosomal recessive lower motor neuron disease with childhood onset
- Autosomal recessive lymphoproliferative disease
- Autosomal recessive malignant osteopetrosis
- Autosomal recessive medullary cystic kidney disease
- Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
- Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
- Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency
- Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency
- Autosomal recessive metaphyseal chondrodysplasia
- Autosomal recessive MSMD due to partial IFNgammaR1 deficiency
- Autosomal recessive MSMD due to partial IFNgammaR2 deficiency
- Autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency
- Autosomal recessive MSMD due to partial interferon gamma receptor 2 deficiency
- Autosomal recessive multiple pterygium syndrome
- Autosomal recessive myogenic AMC
- Autosomal recessive myogenic arthrogryposis multiplex congenita
- Autosomal recessive nail dysplasia
- Autosomal recessive nephronophthisis
- Autosomal recessive non-lethal multiple pterygium syndrome
- Autosomal recessive nonsyndromic intellectual deficit
- Autosomal recessive nonsyndromic neurosensory deafness type DFNB
- Autosomal recessive nonsyndromic sensorineural deafness type DFNB
- Autosomal recessive omodysplasia
- Autosomal recessive optic atrophy, OPA6 type
- Autosomal recessive optic atrophy, OPA7 type
- Autosomal recessive optic atrophy type 3
- Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia
- Autosomal recessive osteopetrosis type 7
- Autosomal recessive palmoplantar hyperkeratosis and congenital alopecia
- Autosomal recessive palmoplantar keratoderma and congenital alopecia
- Autosomal recessive polycystic kidney disease
- Autosomal recessive popliteal pterygium syndrome
- Autosomal recessive posterior column ataxia and retinitis pigmentosa
- Autosomal recessive primary hypomagnesemia with normocalcuria and hypocalcemia
- Autosomal recessive primary microcephaly
- Autosomal recessive progressive external ophthalmoplegia
- Autosomal recessive proximal renal tubular acidosis
- Autosomal recessive pseudohypoaldosteronism type 1
- Autosomal recessive pure HSP
- Autosomal recessive pure spastic paraplegia
- Autosomal recessive pure SPG
- Autosomal recessive pyridoxine-refractory sideroblastic anemia
- Autosomal recessive Robinow syndrome
- Autosomal recessive secondary erythrocytosis, non Chuvash type
- Autosomal recessive secondary erythrocytosis not associated with VHL gene
- Autosomal recessive secondary polycythemia, non Chuvash type
- Autosomal recessive secondary polycythemia not associated with VHL gene
- Autosomal recessive Segawa syndrome
- Autosomal recessive sensory radicular neuropathy
- Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
- Autosomal recessive SLE
- Autosomal recessive spastic ataxia 4
- Autosomal recessive spastic ataxia 5
- Autosomal recessive spastic ataxia - optic atrophy - dysarthria
- Autosomal recessive spastic ataxia type 3
- Autosomal recessive spastic ataxia with leukoencephalopathy
- Autosomal recessive spastic paraplegia - disc herniation
- Autosomal recessive spastic paraplegia type 11
- Autosomal recessive spastic paraplegia type 14
- Autosomal recessive spastic paraplegia type 15
- Autosomal recessive spastic paraplegia type 18
- Autosomal recessive spastic paraplegia type 20
- Autosomal recessive spastic paraplegia type 21
- Autosomal recessive spastic paraplegia type 23
- Autosomal recessive spastic paraplegia type 24
- Autosomal recessive spastic paraplegia type 25
- Autosomal recessive spastic paraplegia type 26
- Autosomal recessive spastic paraplegia type 27
- Autosomal recessive spastic paraplegia type 28
- Autosomal recessive spastic paraplegia type 30
- Autosomal recessive spastic paraplegia type 32
- Autosomal recessive spastic paraplegia type 35
- Autosomal recessive spastic paraplegia type 39
- Autosomal recessive spastic paraplegia type 43
- Autosomal recessive spastic paraplegia type 44
- Autosomal recessive spastic paraplegia type 45
- Autosomal recessive spastic paraplegia type 46
- Autosomal recessive spastic paraplegia type 48
- Autosomal recessive spastic paraplegia type 49
- Autosomal recessive spastic paraplegia type 53
- Autosomal recessive spastic paraplegia type 54
- Autosomal recessive spastic paraplegia type 55
- Autosomal recessive spastic paraplegia type 56
- Autosomal recessive spastic paraplegia type 5A
- Autosomal recessive spastic paraplegia type 7
- Autosomal recessive spinocerebellar ataxia-10
- Autosomal recessive spinocerebellar ataxia-11
- Autosomal recessive spinocerebellar ataxia-12
- Autosomal recessive spinocerebellar ataxia-6
- Autosomal recessive spinocerebellar ataxia-7
- Autosomal recessive spinocerebellar ataxia-9
- Autosomal recessive spondylocostal dysostosis
- Autosomal recessive Stickler syndrome
- Autosomal recessive systemic lupus erythematosus
- Autosomal recessive uncomplicated HSP
- Autosomal recessive uncomplicated spastic paraplegia
- Autosomal recessive uncomplicated SPG
- Autosomal thrombocytopenia with normal platelets
- AUTS2 syndrome
- AVED
- Avellino corneal dystrophy
- Axenfeld-Rieger's anomaly
- Axenfeld-Rieger syndrome
- Axenfeld's anomaly
- Axenfeld syndrome
- Axial mesodermal dysplasia spectrum
- Axial osteosclerosis
- Axial spondylometaphyseal dysplasia
- Axonal Charcot-Marie-Tooth disease with acrodystrophy
- Axonal Charcot-Marie-Tooth disease with pyramidal involvement
- Axonal polyneuropathy associated with IgG/IgM/IgA monoclonal gammopathy
- Ayazi syndrome
- AZOOR
- Azoospermia due to maturation arrest
- Azoospermia due to meiosis defect
- Azoospermia - sinopulmonary infections
- Azorean disease of the nervous system
- Azygos continuation of the inferior caval vein
- Azygos continuation of the inferior vena cava
- Azygos continuation of the IVC











