Syndromic Microphthalmia 11
Disease ID: disease_node_16600
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:614402 |
|---|---|
| Subclassof | DOID_0080636 |
| Data Source | DOID |
| Synonyms | MCOPS11 |
| Doid Label | syndromic microphthalmia 11 |
| Doid Description | A syndromic microphthalmia characterized by microphthalmia, cleft lip and palate, and agenesis of the corpus callosum that has_material_basis_in homozygous or compound heterozygous mutation in VAX1 on chromosome 10q25.3. |
| Disease Node Id | disease_node_16600 |
| Doid Id | DOID_0111804 |
| Label | Syndromic Microphthalmia 11 |
- Outgoing r'ship
SUBCLASS_OFto/from Syndromic Microphthalmia(ID:disease_node_16597) (Disease)