Watson Syndrome
Disease ID: disease_node_19062
Connections displayed (default: 10).
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| Dbxref | MIM:193520 |
|---|---|
| Subclassof | DOID_0050736, DOID_0080690 |
| Data Source | DOID |
| Doid Label | Watson syndrome |
| Doid Description | A RASopathy characterized by pulmonic stenosis, cafe-au-lait macules, decreased intellectual ability, and short stature that has_material_basis_in heterozygous mutation in the NF1 gene on chromosome 17q11.2. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19062 |
| Doid Id | DOID_0070483 |
| Label | Watson Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Rasopathy(ID:disease_node_19055) (Disease)