Noo Syndrome 7
Disease ID: disease_node_19053
Connections displayed (default: 10).
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| Dbxref | ICD10CM:Q87.1, MIM:613706 |
|---|---|
| Subclassof | DOID_0050736, DOID_3490 |
| Data Source | DOID |
| Synonyms | NS7 |
| Doid Label | Noo syndrome 7 |
| Doid Description | A Noo syndrome that has_material_basis_in heterozygous mutation in the BRAF gene. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19053 |
| Doid Id | DOID_0060585 |
| Label | Noo Syndrome 7 |
| Doid Alternate Ids | DOID_0070107 |
- 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)