Isolated Microphthalmia 3
Disease ID: disease_node_16605
Connections displayed (default: 10).
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| Dbxref | ICD10CM:Q11.0, MIM:611038, ORDO:2542 |
|---|---|
| Subclassof | DOID_0050737, DOID_0080637 |
| Data Source | DOID |
| Synonyms | MCOP3 |
| Doid Label | isolated microphthalmia 3 |
| Doid Description | An isolated microphthalmia characterized by clinical anophthalmia and/or microphthalmia that has_material_basis_in compound heterozygous mutation in the RAX gene on chromosome 18q21. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16605 |
| Doid Id | DOID_0060842 |
| Label | Isolated Microphthalmia 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Isolated Microphthalmia(ID:disease_node_16604) (Disease)