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Wolfram syndrome; diabetes insipidus & mellitus with optic atrophy & deafness syndrome (DIDMOAD)
Epidemiology: rare
Genetics:
- autosomal recessive
- associated with mutations in gene for wolframin
Clinical manifestations:
- juvenile onset
- diabetes insipidus
- diabetes mellitus
- optic atrophy
- deafness
- various neurological symptoms
Related
Wolfram syndrome 2
Wolframin (WFS1)
General
genetic syndrome (multisystem disorder)
genetic disease of the endocrine system
Database Correlations
OMIM correlations
MORBIDMAP 606201
References
OMIM :accession 222300