White-Sutton Syndrome
Disease ID: disease_node_16490
Connections displayed (default: 10).
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| Dbxref | MIM:616364 |
|---|---|
| Subclassof | DOID_0060307 |
| Data Source | DOID |
| Synonyms | MRD37, WHSUS, autosomal dominant mental retardation 37 |
| Doid Label | White-Sutton syndrome |
| Doid Description | An autosomal domit intellectual developmental disorder that has_material_basis_in an autosomal domit mutation of the POGZ gene on chromosome 1q21.3. |
| Disease Node Id | disease_node_16490 |
| Doid Id | DOID_0070067 |
| Label | White-Sutton Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Intellectual Developmental Disorder(ID:disease_node_16455) (Disease)