Noo Syndrome 11
Disease ID: disease_node_19048
Connections displayed (default: 10).
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| Dbxref | MIM:618499 |
|---|---|
| Subclassof | DOID_0050736, DOID_3490 |
| Data Source | DOID |
| Synonyms | NS11 |
| Doid Label | Noo syndrome 11 |
| Doid Description | A Noo syndrome characterized by clinical characteristics of Noo syndrome, varying impairment of intellectual development, and cardiac hypertrophy that has_material_basis_in heterozygous mutation in the MRAS gene on chromosome 3q22.3. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19048 |
| Doid Id | DOID_0112169 |
| Label | Noo Syndrome 11 |
- Outgoing r'ship
SUBCLASS_OFto/from Noonan Syndrome(ID:disease_node_5622) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)