Cone-Rod Dystrophy 20
Disease ID: disease_node_16581
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| Dbxref | MIM:615973 |
|---|---|
| Subclassof | DOID_0050572 |
| Data Source | DOID |
| Synonyms | CORD20 |
| Doid Label | cone-rod dystrophy 20 |
| Doid Description | A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the POC1B gene on chromosome 12q21. |
| Disease Node Id | disease_node_16581 |
| Doid Id | DOID_0111026 |
| Label | Cone-Rod Dystrophy 20 |
- Outgoing r'ship
SUBCLASS_OFto/from Cone-Rod Dystrophy(ID:disease_node_16580) (Disease)