header logo image header logo text
Downloads Login
Research
General Information
ZIRC
OBO ID: DOID:0110629
Term Name: Wolfram syndrome 1 Search Ontology:
Synonyms:
  • diabetes mellitus AND insipidus with optic atrophy AND deafness
  • WFS1
Definition: An autosomal recessive disease that is characterized by diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the WFS1 gene on chromosome 4p16.1. https://www.ncbi.nlm.nih.gov/pubmed/21538838
References:
Ontology: Human Disease   (DOID:0110629)
OTHER Wolfram syndrome 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WFS1 Wolfram syndrome 1 222300
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None