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Disease Ontology Browser
Frasier syndrome (DOID:0050438)
Alliance: disease page
Alt IDs: OMIM:136680, MESH:D052159, NCI:C122805, UMLS_CUI:C0950122
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.13
The Jackson Laboratory