Frasier Syndrome
Disease ID: disease_node_11506
Connections displayed (default: 10).
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| Dbxref | GARD:2375, MESH:D052159, MIM:136680, NCI:C122805, SNOMEDCT_US_2023_03_01:445431000, UMLS_CUI:C0950122 |
|---|---|
| Subclassof | DOID_0050736, DOID_225 |
| Data Source | DOID, MESH |
| Mesh Id | D052159 |
| Mesh Label | Frasier Syndrome |
| Mesh Subclassof | D030342, D007676, D058490 |
| Doid Label | Frasier syndrome |
| Doid Description | 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. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_11506 |
| Doid Id | DOID_0050438 |
| Label | Frasier Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)