OBO ID: DOID:0050438 |
Term Name: | Frasier syndrome | Search Ontology: | |
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Definition: | An autosomal dominant disease 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 | ||
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Ontology: | Human Disease (DOID:0050438) |