Search Ontology:
Human Disease
Frasier syndrome
- Term ID
- DOID:0050438
- 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
- MIM:136680
- Ontology
- Human Disease ( DOID:0050438 )
- is a type of
Other Pages
Genes Involved
Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
---|---|---|---|---|
WT1 | Frasier syndrome | Frasier syndrome | 136680 |
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Zebrafish Models
No data available