Cone-Rod Dystrophy 2
Disease ID: disease_node_16593
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| Dbxref | GARD:6145, MIM:120970 |
|---|---|
| Subclassof | DOID_0050572 |
| Data Source | DOID |
| Synonyms | CORD2, CRD2, RCRD2, cone-rod retinal dystrophy 2, retinal cone-rod dystrophy 2 |
| Doid Label | cone-rod dystrophy 2 |
| Doid Description | A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13. |
| Disease Node Id | disease_node_16593 |
| Doid Id | DOID_0111005 |
| Label | Cone-Rod Dystrophy 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Cone-Rod Dystrophy(ID:disease_node_16580) (Disease)