Orphanet: Diseases list
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L1CAM syndrome L1 syndrome L-2-HGA L-2-hydroxyglutaric acidemia L-2-hydroxyglutaric aciduria Laband syndrome Labrune syndrome L-ACAOS Lacrimal drainage system anomaly Lacrimal drainage system anomaly of genetic origin Lacrimoauriculodentodigital syndrome Lacrimoauriculoradiodental syndrome La Crosse encephalitis Lactate dehydrogenase A deficiency Lactate dehydrogenase B deficiency Lactotroph adenoma LAD LAD-1 variant Ladda-Zonana-Ramer syndrome LADD syndrome LAD-I LAD-II LAD-III LAEB Lafora disease Lagophthalmia-cleft lip and palate syndrome LAI Laing early-onset distal myopathy LAL deficiency LAM LAMA2-related muscular dystrophy LAMA5-related multisystemic syndrome Lambert-Eaton myasthenic syndrome Lambert syndrome Lamb-Shaffer syndrome Lamellar ichthyosis Laminin subunit alpha 2-related congenital muscular dystrophy Laminin subunit alpha 2-related late-onset muscular dystrophy Laminin subunit alpha 2-related LGMD R23 Laminin subunit alpha 2-related limb-girdle muscular dystrophy R23 Laminin subunit alpha 2-related muscular dystrophy Laminopathy Laminopathy with lipodystrophy Laminopathy with peripheral neuropathy Laminopathy with premature aging Laminopathy with striated muscle involvement LAMM syndrome Landau-Kleffner syndrome Landing disease Landouzy-Dejerine dystrophy Landouzy-Dejerine myopathy Lane disease Langer-Giedion syndrome Langerhans cell granulomatosis Langerhans cell histiocytosis Langerhans cell sarcoma Langer mesomelic dysplasia Laparoschisis LARD syndrome Large cell lymphoma of the mediastinum Large congenital melanocytic nevus Large granular lymphocyte leukemia L-Arginine:glycine amidinotransferase deficiency Laron-like syndrome Laron syndrome Laron syndrome with immunodeficiency Laron-type dwarfism Larsen-like osseous dysplasia-short stature syndrome Larsen-like syndrome, B3GAT3 type Larsen syndrome Laryngeal abductor paralysis Laryngeal abductor paralysis-intellectual disability syndrome Laryngeal and ocular granulation tissue in children from the Indian subcontinent syndrome Laryngeal neuroendocrine tumor Laryngocele Laryngo-onycho-cutaneous syndrome Laryngotracheal angioma Laryngotracheoesophageal cleft Laryngo-tracheo-esophageal cleft Laryngotracheoesophageal cleft type 0 Laryngo-tracheo-esophageal cleft type 0 Laryngotracheoesophageal cleft type 1 Laryngo-tracheo-esophageal cleft type 1 Laryngotracheoesophageal cleft type 2 Laryngo-tracheo-esophageal cleft type 2 Laryngotracheoesophageal cleft type 3 Laryngo-tracheo-esophageal cleft type 3 Laryngotracheoesophageal cleft type 4 Laryngo-tracheo-esophageal cleft type 4 Laryngo-tracheo-esophageal diastema Larynx anomaly Larynx atresia Lassa fever Lassa hemorrhagic fever Late hereditary endothelial dystrophy Late infantile CACH syndrome Late-infantile GM1 gangliosidosis Late-infantile/juvenile Krabbe disease Late infantile NCL Late infantile neuronal ceroid lipofuscinosis Late-onset ataxia with dementia Late-onset benign childhood occipital epilepsy Late-onset citrullinemia type 1 Late-onset citrullinemia type I Late-onset distal crystallinopathy Late-onset distal myopathy, Markesbery-Griggs type Late-onset familial encephalopathy with neuroserpin inclusion bodies Late-onset familial hyperreninemic hypoaldosteronism Late-onset familial hypoaldosteronism Late-onset focal dermal elastosis Late-onset infantile spasms Late-onset isolated ACTH deficiency Late-onset JEB Late-onset junctional epidermolysis bullosa Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Late-onset multiple carboxylase deficiency Late-onset myotonic dystrophy type 1 Late-onset nephronophthisis Late-onset primary lymphedema without systemic or visceral involvement Late-onset retinal degeneration Late-onset scapuloperoneal muscular dystrophy with hyaline bodies Late-onset scapuloperoneal syndrome, myopathic type Late-onset spinal motor neuronopathy Late-onset SPMD with hyaline bodies Late-onset Steinert disease Late-onset Steinert myotonic dystrophy Lateral facial cleft Lateralization defect Lateral meningocele syndrome Lathosterolosis Lattice corneal dystrophy type 1 Lattice corneal dystrophy type I Laubry-Pezzi syndrome Launois-Bensaude lipomatosis Laurence-Moon syndrome Laurin-Sandrow syndrome Lawrence-Seip syndrome Lawrence syndrome Laxova-Opitz syndrome LBSL LBWC syndrome LC LCAT deficiency LCC LCCS LCCS1 LCCS2 LCCS3 LCCS5 LCD1 LCDD LCDI LCH LCHADD LCHAD deficiency LCM L-CMD LCMN LCPS L-CPT1 deficiency L-CPTI deficiency LDD LDH deficiency LDH-H subunit deficiency LDH-M subunit deficiency Lead intoxication Lead poisoning Learman syndrome Leber congenital amaurosis Leber hereditary optic neuropathy Leber miliary aneurysm Leber optic atrophy Leber plus disease LECD Lecithin-cholesterol acyltransferase deficiency Ledderhose disease Left coronary artery from right aortic sinus Left renal vein entrapment syndrome Left sided atrial isomerism Left ventricular hypertrabeculation Left ventricular noncompaction Left ventricular-to-right atrial communication Leg duplication-mirror foot syndrome Legg-Calvé-Perthes disease Legionellosis Legionnaires disease Legius syndrome Lehman syndrome Leichtman-Wood-Rohn syndrome Leigh disease Leigh disease with leukodystrophy Leigh disease with myopathy Leigh disease with nephrotic syndrome Leigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndrome Leigh-like encephalopathy-optic atrophy-peripheral neuropathy syndrome Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency Leigh syndrome Leigh syndrome due to PC deficiency Leigh syndrome due to pyruvate carboxylase deficiency Leigh syndrome, French-Canadian type Leigh syndrome, Saguenay-Lac-Saint-Jean type Leigh syndrome with cardiomyopathy Leigh syndrome with leukodystrophy Leigh syndrome with nephrotic syndrome Leiner disease Leiomyomatosis peritonealis disseminate Leiomyosarcoma Leiomyosarcoma of small intestine Leiomyosarcoma of the cervix uteri Leiomyosarcoma of the corpus uteri Leishmaniasis Lelis syndrome Lemierre postanginal sepsis Lemierre syndrome Lenk-Ploski syndrome Lennox-Gastaut syndrome Lens-induced endophthalmitis Lens-induced iridocyclitis Lens-induced uveitis Lens position anomaly Lens position anomaly of genetic origin Lens shape anomaly Lens size anomaly Lens size anomaly of genetic origin Lenz-Majewski hyperostotic dwarfism Lenz microphthalmia LEOPARD syndrome Lepore-beta-thalassemia syndrome Leprechaunism Leprosy Leptomeningeal melanomatosis Leptomyelolipoma Leptospirosis Leri pleonosteosis Léri-Weill dyschondrosteosis Léri-Weill syndrome Lesch-Nyhan syndrome Lethal acantholytic epidermolysis bullosa Lethal arteriopathy syndrome due to fibulin-4 deficiency Lethal ataxia with deafness and optic atrophy Lethal ataxia with hearing loss and optic atrophy Lethal brain and heart developmental defects Lethal chondrodysplasia Lethal congenital contracture syndrome Lethal congenital contracture syndrome type 1 Lethal congenital contracture syndrome type 2 Lethal congenital contracture syndrome type 3 Lethal congenital contracture syndrome type 5 Lethal faciocardiomelic dysplasia Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Lethal hemolytic anemia-genital anomalies syndrome Lethal hydranencephaly-diaphragmatic hernia syndrome Lethal hydrocephalus-cardiac malformation-dense bones syndrome Lethal hyperkeratosis-contracture syndrome Lethal infantile mitochondrial disease Lethal infantile mitochondrial myopathy Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome Lethal Kniest-like dysplasia Lethal Larsen-like syndrome Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Lethal midline granuloma Lethal multiple congenital anomalies/dysmorphic syndrome Lethal multiple pterygium syndrome Lethal neonatal rigidity-multifocal seizure syndrome Lethal neonatal spasticity-epileptic encephalopathy syndrome Lethal neurodegenerative disorder due to copper transport defect Lethal occipital encephalocele-skeletal dysplasia syndrome Lethal omphalocele-cleft palate syndrome Lethal osteogenesis imperfecta Lethal osteosclerotic bone dysplasia Lethal polymalformative syndrome, Boissel type Lethal popliteal pterygium syndrome Lethal recessive chondrodysplasia Lethal restrictive dermopathy Lethal skeletal dysplasia-fetal akinesia-contractures-thoracic dysplasia-pulmonary hypoplasia syndrome Lethal tight skin-contracture syndrome Letrozole toxicity Leukemic reticuloendotheliosis Leukemic reticuloendotheliosis variant Leukocyte adhesion deficiency Leukocyte adhesion deficiency-1 variant Leukocyte adhesion deficiency type I Leukocyte adhesion deficiency type II Leukocyte adhesion deficiency type III Leukocyte chemotactic factor-2 amyloidosis Leukodystrophy Leukodystrophy due to alkaline ceramidase 3 deficiency Leukodystrophy with oligodontia Leukoencephalopathy-dystonia-motor neuropathy syndrome Leukoencephalopathy-metaphyseal chondrodysplasia syndrome Leukoencephalopathy-palmoplantar keratoderma syndrome Leukoencephalopathy-SEMD syndrome Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Leukoencephalopathy with bilateral anterior temporal lobe cysts Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome Leukoencephalopathy with brain stem and spinal cord involvement-lactate elevation syndrome Leukoencephalopathy with calcifications and cysts Leukoencephalopathy with mild cerebellar ataxia and white matter edema Leukoencephalopathy with vanishing white matter Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome Leukonychia totalis Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome Leukonychia totalis-trichilemmal cysts-ciliary dystrophy syndrome Leukotriene C4 synthase deficiency Levic-Stefanovic-Nikolic syndrome Levine-Critchley syndrome Levocardia Levocardia with situs inversus Levo-transposition of the great arteries Levy-Hollister syndrome Lewandowsky-Lutz syndrome Lewis-Sumner syndrome Leydig cell hypoplasia Leydig cell hypoplasia due to complete LH receptor inactivation Leydig cell hypoplasia due to complete LH resistance Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation Leydig cell hypoplasia due to complete luteinizing hormone resistance Leydig cell hypoplasia due to LHB deficiency Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency Leydig cell hypoplasia due to partial LH receptor inactivation Leydig cell hypoplasia due to partial LH resistance Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation Leydig cell hypoplasia due to partial luteinizing hormone resistance LF L-ferritin deficiency LGL syndrome L-glyceric aciduria LGMD LGMD1A LGMD1D LGMD1F LGMD1G LGMD1H LGMD1I LGMD2A LGMD2B LGMD2C LGMD2D LGMD2E LGMD2F LGMD2G LGMD2H LGMD2I LGMD2J LGMD2K LGMD2L LGMD2M LGMD2N LGMD2O LGMD2P LGMD2Q LGMD2S LGMD2T LGMD2U LGMD2W LGMD2X LGMD2Y LGMD2Z LGMD due to alpha-sarcoglycan deficiency LGMD due to beta-sarcoglycan deficiency LGMD due to delta-sarcoglycan deficiency LGMD due to dysferlin deficiency LGMD due to FKRP deficiency LGMD due to gamma-sarcoglycan deficiency LGMD due to POMK deficiency LGMD due to telethonin deficiency LGMD due to TRIM32 deficiency LGMD type 1D LGMD type 1F LGMD type 1G LGMD type 2A LGMD type 2B LGMD type 2C LGMD type 2D LGMD type 2E LGMD type 2F LGMD type 2G LGMD type 2H LGMD type 2I LGMD type 2J LGMD type 2K LGMD type 2L LGMD type 2M LGMD type 2N LGMD type 2O LGMD type 2P LGMD type 2Q LGMD type 2S LGMD type 2T LGMD type 2U LGMD type 2W LGMD type 2X LGMD type 2Y LGMD type 2Z LGMD type D4 LGMD type R23 LGMD type R24 LHCDD Lhermitte-Duclos disease LHON LHON plus disease LI Liberfarb syndrome Lichen amyloidosis Lichen amyloidosus Lichen follicularis Lichen myxedematosus Lichenoid melanodermatitis Lichen planopilaris Lichen planus actinus Lichen planus follicularis Lichen planus pemphigoides Lichen planus pigmentosa Lichen planus pigmentosus Lichen planus pigmentosus inversus Lichen planus subtropicus Lichen planus tropicus Lichtenstein-Knorr syndrome Lichtenstein syndrome Liddle syndrome Liebenberg syndrome Li-Fraumeni syndrome LIG4 syndrome Ligase 4 syndrome Light and heavy chain deposition disease Light-chain amyloidosis Light chain deposition disease Limbal stem cell deficiency Limb body wall complex Limb-girdle muscular dystrophy Limb-girdle muscular dystrophy 2X Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency Limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency Limb-girdle muscular dystrophy due to calpain deficiency Limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency Limb-girdle muscular dystrophy due to dysferlin deficiency Limb-girdle muscular dystrophy due to FKRP deficiency Limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency Limb-girdle muscular dystrophy due to myotilin deficiency Limb-girdle muscular dystrophy due to POMK deficiency Limb-girdle muscular dystrophy due to telethonin deficiency Limb-girdle muscular dystrophy due to TRIM32 deficiency Limb-girdle muscular dystrophy-intellectual disability syndrome Limb-girdle muscular dystrophy type 1D Limb-girdle muscular dystrophy type 1F Limb-girdle muscular dystrophy type 1G Limb-girdle muscular dystrophy type 2A Limb-girdle muscular dystrophy type 2B Limb-girdle muscular dystrophy type 2C Limb-girdle muscular dystrophy type 2D Limb-girdle muscular dystrophy type 2E Limb-girdle muscular dystrophy type 2F Limb-girdle muscular dystrophy type 2G Limb-girdle muscular dystrophy type 2H Limb-girdle muscular dystrophy type 2I Limb-girdle muscular dystrophy type 2J Limb-girdle muscular dystrophy type 2K Limb-girdle muscular dystrophy type 2L Limb-girdle muscular dystrophy type 2N Limb-girdle muscular dystrophy type 2O Limb-girdle muscular dystrophy type 2P Limb-girdle muscular dystrophy type 2Q Limb-girdle muscular dystrophy type 2S Limb-girdle muscular dystrophy type 2T Limb-girdle muscular dystrophy type 2U Limb-girdle muscular dystrophy type 2W Limb-girdle muscular dystrophy type 2Z Limb-girdle muscular dystrophy type D4 Limb-girdle muscular dystrophy type R24 Limb-girdle muscular dystrophy with epidermolysis bullosa simplex Limb-girdle muscular dystrophy with Paget disease of bone Limbic encephalitis Limbic encephalitis associated with antibodies to cell membrane antigens Limbic encephalitis-neuromyotonia-hyperhidrosis-polyneuropathy syndrome Limbic encephalitis with caspr2 antibodies Limbic encephalitis with dipeptidyl-peptidase 6 antibodies Limbic encephalitis with DPP6 antibodies Limbic encephalitis with DPPX antibodies Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies Limbic encephalitis with LGI1 antibodies Limbic encephalitis with neurexin-3 antibodies Limbic encephalitis with NMDA receptor antibodies Limbic encephalitis with N-methyl-D-aspartate receptor antibodies Limb-mammary syndrome Limb, scalp and skull defects LIMD Limit dextrinosis Limited cutaneous systemic scleroderma Limited cutaneous systemic sclerosis Limited systemic sclerosis LIMM LIMS2-related LGM LIMS2-related limb-girdle muscular dystrophy LINCL Lindau disease Lindsay-Burn syndrome Linear and whorled nevoid hypermelanosis Linear atrophoderma of Moulin Linear focal dermal elastosis Linear focal elastosis Linear hamartoma syndrome Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies Linear IgA dermatosis Linear lichen planus Linear LP Linear nevus sebaceus syndrome Linear verrucous nevus syndrome Linitis plastica of the stomach LIPE-related familial partial lipodystrophy LIPE-related FPLD Lipidosis with triglyceride storage disease Lipid storage disease Lipid storage myopathy Lipoamide dehydrogenase deficiency Lipoate biosynthesis defect Lipoatrophia semicircularis Lipoatrophic diabetes Lipoatrophy caused by injected drug Lipoblastoma Lipodystrophia centrifugalis abdominalis infantilis Lipodystrophy due to peptidic growth factors deficiency Lipodystrophy-intellectual disability-deafness syndrome Lipodystrophy-intellectual disability-hearing loss syndrome Lipodystrophy-Rieger anomaly-diabetes syndrome Lipoic acid biosynthesis defect Lipoic acid synthetase deficiency Lipoid dermatoarthritis Lipoid proteinosis Lipoma associated with neurospinal dysraphism Lipomatosis dolorosa Lipomatous mesenteritis Lipomucopolysaccharidosis Lipomyelomeningocele Lipoprotein glomerulopathy Liposarcoma Liposclerotic mesenteritis Lipoyl transferase 1 deficiency Lipoyl transferase 2 deficiency Lip-pit syndrome Lisch epithelial corneal dystrophy Lisker-Garcia-Ramos syndrome Lison syndrome Lissencephaly Lissencephaly due to 17p13.3 deletion Lissencephaly due to LIS1 mutation Lissencephaly due to TUBA1A mutation Lissencephaly syndrome, Norman-Roberts type Lissencephaly type 1 Lissencephaly type 1 due to doublecortin gene mutation Lissencephaly type 2 Lissencephaly type 2 with muscular and ocular involvement Lissencephaly type 2 without muscular or eye involvement Lissencephaly type 2 without muscular or ocular involvement Lissencephaly type 3 Lissencephaly type 3-familial fetal akinesia sequence syndrome Lissencephaly type 3-metacarpal bone dysplasia syndrome Lissencephaly with cerebellar hypoplasia Lissencephaly with cerebellar hypoplasia type A Lissencephaly with cerebellar hypoplasia type B Lissencephaly with cerebellar hypoplasia type C Lissencephaly with cerebellar hypoplasia type D Lissencephaly with cerebellar hypoplasia type E Lissencephaly with cerebellar hypoplasia type F Listeria infection Listeriosis Livedoid vasculopathy Livedo racemosa-cerebrovascular accident syndrome Livedo reticularis-cerebrovascular accident syndrome Livedo reticularis with summer ulcerations Liver adenomatosis Liver disease-retinitis pigmentosa-polyneuropathy-epilepsy syndrome Liver glycogen phosphorylase deficiency LKS LM LMNA-related cardiocutaneous progeria syndrome LMNA-related congenital muscular dystrophy LMPS LMS Lobar holoprosencephaly Lobstein disease Localized AL amyloidosis Localized Castleman disease Localized deciduous skin Localized epidermolysis bullosa simplex Localized fibrosing scleroderma Localized junctional epidermolysis bullosa, non-Herlitz type Localized lichen myxedematosus Localized lichen myxedematosus with mixed features of different subtypes Localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms Localized lipodystrophy Localized pagetoid reticulosis Localized PSS Localized pustular psoriasis Localized scleroderma Locked-in syndrome LOC syndrome Loeffler endocarditis Loeys-Dietz syndrome LOGIC syndrome Logopenic primary progressive aphasia Logopenic progressive aphasia Logopenic variant PPA Loiasis Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Long eyelashes-intellectual disability syndrome Longitudinal limb defect Longitudinal meromelia Longitudinal vaginal septum Longman-Tolmie syndrome Long QT interval-deafness syndrome Long QT interval-hearing loss syndrome Long QT syndrome-syndactyly syndrome Long QT syndrome type 7 Long QT syndrome type 8 Loose anagen syndrome LOPD Lopes-Gorlin syndrome Lopes-Marques de Faria syndrome LORD Loricrin keratoderma LOSMoN Loucks-Innes syndrome Lou Gehrig disease Louis-Bar syndrome Lowe disease Lowe-Kohn-Cohen syndrome Lowe oculocerebrorenal dystrophy Lowe oculo-cerebro-renal dystrophy Lowe oculo-cerebro-renal syndrome Lower body hemangioma-urogenital anomalies-myelopathy-bony deformities-anorectal and arterial malformations-renal anomalies syndrome Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy Lower limb hypertrophy Lower limb malformation-hypospadias syndrome Lower lip fistula Lower motor neuron syndrome with late-adult onset Lowe syndrome Low-flow priapism Low-grade astrocytoma Low-grade neuroendocrine tumor of the corpus uteri Low-grade neuroendocrine tumor of the uterine corpus Low isolated anorectal malformation Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis Lown-Ganong-Levine syndrome Low phospholipid-associated cholelithiasis Lowry-MacLean syndrome Lowry syndrome Lowry-Wood syndrome Lowry-Yong syndrome LPA LPAC LPD LPG LPI LPL deficiency LPP LPP LP pemphigoides LP pigmentosa LP pigmentosus LQT7 LQT8 LQT8 type 1 LQT8 type 2 LQTS LRP5-related primary osteoporosis LTBL LTC4 synthase deficiency LTEC LTEC0 LTEC1 LTEC2 LTEC3 LTEC4 LTEC I LTEC II LTEC III LTEC IV L-transposition of the great arteries Lubag Lubag syndrome Lubani-Al Saleh-Teebi syndrome Lubinsky syndrome Lucey-Driscoll syndrome Lujan-Fryns syndrome Lujan syndrome Lujo hemorrhagic fever LUMBAR syndrome Lumbosacral spina bifida aperta Lumbosacral spina bifida cystica Lunatomalacia Lundberg syndrome Lung agenesis-heart defect-thumb anomalies syndrome Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome Lupus erythematosus panniculitis Lupus erythematosus profundus Lupus erythematosus tumidus Luteal-phase-dependent febrile episode Luteal-phase-dependent periodic fever Luteinizing hormone-releasing hormone deficiency with ataxia LUTO Lutz-Lewandowsky epidermodysplasia verruciformis LVNC LWNH Lyell syndrome LYG Lyme borreliosis Lyme disease Lymphangioleiomyomatosis Lymphangioma Lymphatic filariasis Lymphedema-atrial septal defects-facial changes syndrome Lymphedema-cerebral arteriovenous anomaly syndrome Lymphedema-distichiasis syndrome Lymphedema-hypoparathyroidism syndrome Lymphedema-lymphangiectasia-intellectual disability syndrome Lymphedema-posterior choanal atresia syndrome Lymphedema with yellow nails Lymphoblastoid variant of NK-cell lymphoma Lymphocytic hypereosinophilic syndrome Lymphocytic interstitial pneumonia Lymphocytic variant HES Lymphoepithelial-like carcinoma Lymphogranulomatosis X Lymphoid hemopathy Lymphoid HES Lymphoid interstitial pneumonia Lymphoma Lymphomatoid granulomatosis Lymphomatoid papulosis Lymphoplasmacytic inflammatory pseudotumor of the liver Lymphoplasmacytic lymphoma without IgM production Lymphoplasmacytic lymphoma without Immunoglobulin M production Lymphoplasmacytic sclerosing pancreatitis Lymphoproliferative disease associated with primary immune disease Lymphoproliferative syndrome Lynch-Lee-Murday syndrome Lynch syndrome Lyngstadaas syndrome LyP Lysine alpha-ketoglutarate reductase deficiency Lysinuric protein intolerance Lysosomal acid lipase deficiency Lysosomal acid phosphatase deficiency Lysosomal alpha-D-mannosidase deficiency Lysosomal alpha-D-mannosidase deficiency, adult form Lysosomal alpha-D-mannosidase deficiency, infantile form Lysosomal disease Lysosomal disease with epilepsy Lysosomal disease with hypertrophic cardiomyopathy Lysosomal disease with restrictive cardiomyopathy Lysosomal glycogen storage disease Lysosomal glycogen storage disease with normal acid maltase activity Lysosomal membrane cobalamin transporter deficiency Lysosomal storage disease with skeletal involvement Lysozyme amyloidosis Lysyl hydroxylase-deficient EDS Lytico-Bodig disease
