ZFIN Human Disease: Frasier syndrome

OBO ID: DOID:0050438

Term Name:	Frasier syndrome		Search Ontology:
Synonyms:
Definition:	A syndrome that is characterized by gonadal dysgenesis, streak gonads, progressive focal segmental glomerulonephropathy and the development of urogenital cancers that is the result of mutation in the WT1 gene. https://ghr.nlm.nih.gov/condition/frasier-syndrome
References:	GARD:2375 MESH:D052159 NCI:C122805 OMIM:136680 SNOMEDCT_US_2020_09_01:445431000 UMLS_CUI:C0950122
Ontology:	Human Disease (DOID:0050438)

Relationships

is a type of:	autosomal dominant disease syndrome autosomal dominant disease syndrome Show first 5 Terms

OTHER Frasier syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
WT1	wt1b wt1a	Frasier syndrome	136680

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None