Neurooculocardiogenitourinary Syndrome
Disease ID: disease_node_20019
Connections displayed (default: 10).
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| Dbxref | MIM:618652 |
|---|---|
| Subclassof | DOID_0050736, DOID_225 |
| Data Source | DOID |
| Synonyms | NOCGUS |
| Doid Label | neurooculocardiogenitourinary syndrome |
| Doid Description | A syndrome characterized by impaired growth and anomalies of the ocular, craniofacial, neurologic, cardiovascular, genitourinary, skeletal, and gastrointestinal systems that has_material_basis_in heterozygous mutation in the WDR37 gene on chromosome 10p15.3. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_20019 |
| Doid Id | DOID_0111675 |
| Label | Neurooculocardiogenitourinary 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)