ZFIN Human Disease: Wolfram syndrome

OBO ID: DOID:10632

Term Name:	Wolfram syndrome		Search Ontology:
Synonyms:	DIDMOAD WFS
Definition:	A syndrome that is characterized by diabetes mellitus, optic atrophy, and deafness. http://en.wikipedia.org/wiki/Wolfram_syndrome
References:	GARD:7898 MESH:D014929 NCI:C35133 ORDO:3463 SNOMEDCT_US_2023_03_01:70694009 UMLS_CUI:C0043207
Ontology:	Human Disease ( DOID:10632 )

Relationships

is a type of:	syndrome syndrome Show first 5 Terms
has subtype:	autosomal dominant Wolfram syndrome Wolfram syndrome 1 Wolfram syndrome 2 Wolfram syndrome, mitochondrial form autosomal dominant Wolfram syndrome Wolfram syndrome 1 Wolfram syndrome 2 Wolfram syndrome, mitochondrial form Show first 5 Terms

OTHER Wolfram syndrome PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS

Fish	Conditions	Citations
wfs1b^{sa16422/sa16422} (AB)	standard conditions	Cairns et al., 2021
wfs1a^{sa11465/sa11465}; wfs1b^{sa16422/sa16422}	standard conditions	Crouzier et al., 2022

PHENOTYPE No data available

CITATIONS (2)