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43 Result(s)

ORPHA:1133   (Disorder)   AREDYLD syndrome

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Synonym(s) : Acrorenal defect-ectodermal dysplasia-diabetes syndrome

ORPHA:95626   (Subtype of disorder)   Acquired central diabetes insipidus

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Synonym(s) : Acquired neurogenic diabetes insipidus

ORPHA:79086   (Disorder)   Acquired generalized lipodystrophy

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Synonym(s) : Acquired lipoatrophic diabetes

ORPHA:3143   (Disorder)   Autoimmune polyendocrinopathy type 2

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Synonym(s) : Autoimmune thyroid disease and/or type 1 diabetes-Addison disease syndrome

ORPHA:1227   (Disorder)   Bangstad syndrome

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Synonym(s) : Ataxia-diabetes-goiter-gonadal insufficiency syndrome

ORPHA:528   (Disorder)   Berardinelli-Seip congenital lipodystrophy

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Synonym(s) : Lipoatrophic diabetes

ORPHA:178029   (Disorder)   Central diabetes insipidus

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Synonym(s) : Neurogenic diabetes insipidus

ORPHA:79134   (Disorder)   DEND syndrome

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Synonym(s) : Developmental delay-epilepsy-neonatal diabetes syndrome

ORPHA:93111   (Subtype of disorder)   HNF1B-related autosomal dominant tubulointerstitial kidney disease

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Synonym(s) : Maturity-onset diabetes of the young type 5 ; Renal dysfunction-early-onset diabetes syndrome

ORPHA:30925   (Subtype of disorder)   Hereditary central diabetes insipidus

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Synonym(s) : Hereditary neurogenic diabetes insipidus

ORPHA:3044   (Disorder)   Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome

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Keyword(s) : Mental retardation-dysmorphism-hypogonadism-diabetes mellitus syndrome

ORPHA:99989   (Subtype of disorder)   Intermediate DEND syndrome

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Synonym(s) : Developmental delay-epilepsy-neonatal diabetes syndrome, intermediate form

ORPHA:445062   (Disorder)   Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome

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Synonym(s) : Combined cerebellar and peripheral ataxia-hearing loss-diabetes mellitus syndrome

ORPHA:552   (Disorder)   MODY

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Synonym(s) : Maturity-onset diabetes of the young

ORPHA:225   (Disorder)   Maternally-inherited diabetes and deafness

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Synonym(s) : Mitochondrial diabetes

ORPHA:224   (Group of disorders)   Neonatal diabetes mellitus

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ORPHA:181381   (Group of disorders)   Other rare diabetes mellitus

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ORPHA:99885   (Disorder)   Permanent neonatal diabetes mellitus

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Synonym(s) : Monogenic diabetes of infancy

ORPHA:391408   (Disorder)   Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome

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Keyword(s) : Primary microcephaly-mild mental retardation-young-onset diabetes syndrome

ORPHA:101952   (Group of disorders)   Rare diabetes mellitus

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ORPHA:181371   (Group of disorders)   Rare diabetes mellitus type 1

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Synonym(s) : Rare insulin-dependent diabetes mellitus

ORPHA:181376   (Group of disorders)   Rare diabetes mellitus type 2

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Synonym(s) : Rare insulin-independent diabetes mellitus

ORPHA:183625   (Group of disorders)   Rare genetic diabetes mellitus

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ORPHA:3163   (Disorder)   SHORT syndrome

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Synonym(s) : Lipodystrophy-Rieger anomaly-diabetes syndrome

ORPHA:49827   (Disorder)   Thiamine-responsive megaloblastic anemia syndrome

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Synonym(s) : Thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness

ORPHA:99886   (Disorder)   Transient neonatal diabetes mellitus

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Keyword(s) : 6q24 transient neonatal diabetes mellitus

ORPHA:1667   (Disorder)   Wolcott-Rallison syndrome

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Synonym(s) : Early-onset diabetes mellitus with multiple epiphyseal dysplasia

ORPHA:3463   (Disorder)   Wolfram syndrome

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Synonym(s) : Diabetes insipidus-diabetes mellitus-optic atrophy-deafness syndrome

ORPHA:3464   (Disorder)   Woodhouse-Sakati syndrome

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Synonym(s) : Diabetes-hypogonadism-deafness-intellectual disability syndrome