Noo Syndrome 12
Disease ID: disease_node_19047
Connections displayed (default: 10).
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| Dbxref | MIM:618624 |
|---|---|
| Subclassof | DOID_0050736, DOID_3490 |
| Data Source | DOID |
| Synonyms | NS12 |
| Doid Label | Noo syndrome 12 |
| Doid Description | A Noo syndrome characterized by macrocephaly, facial anomalies including hypertelorism, downslanting palpebral fissures, and low-set ears, and other Noo syndrome features that has_material_basis_in heterozygous mutation in the RRAS2 gene on chromosome 11p15.2. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19047 |
| Doid Id | DOID_0112170 |
| Label | Noo Syndrome 12 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Noonan Syndrome(ID:disease_node_5622) (Disease)