Isolated Microphthalmia 7
Disease ID: disease_node_16609
Connections displayed (default: 10).
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| Dbxref | ICD10CM:Q11.0, MIM:613704, ORDO:2542 |
|---|---|
| Subclassof | DOID_0050736, DOID_0080637 |
| Data Source | DOID |
| Synonyms | MCOP7 |
| Doid Label | isolated microphthalmia 7 |
| Doid Description | An isolated microphthalmia characterized by unilateral microphthalmia that has_material_basis_in caused by mutation in the GDF3 gene on chromosome 12p13. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16609 |
| Doid Id | DOID_0060838 |
| Label | Isolated Microphthalmia 7 |
- Outgoing r'ship
SUBCLASS_OFto/from Isolated Microphthalmia(ID:disease_node_16604) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)