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Wolfram syndrome

Disease Export to PDF
Name:
Wolfram syndrome
Description:
A rare, genetic, endocrine disorder characterized by type I diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs.
ORPHAcode:
3463
Synonyms:
DIDMOAD syndrome
Diabetes insipidus-diabetes mellitus-optic atrophy-deafness syndrome
Diabetes insipidus-diabetes mellitus-optic atrophy-hearing loss syndrome
XREF(s):
Orphanet
ICD-10
MeSH
OMIM
OMIM
OMIM
Analyte(s):
WFS1
CISD2
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14