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ZIRC
OBO ID: DOID:0050438
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Term Name: Frasier syndrome Search Ontology:
Synonyms:
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
References:
Ontology: Human Disease   (DOID:0050438)
Relationships
is a type of:
OTHER Frasier syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WT1 Frasier syndrome 136680
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None