Cone-Rod Dystrophy 24
Disease ID: disease_node_16594
Connections displayed (default: 10).
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| Dbxref | MIM:620342 |
|---|---|
| Subclassof | DOID_0050572, DOID_0050736 |
| Data Source | DOID |
| Doid Label | cone-rod dystrophy 24 |
| Doid Description | A cone-rod dystrophy that is characterized by night blindness, defective color vision, and reduced visual acuity and that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16594 |
| Doid Id | DOID_0081449 |
| Label | Cone-Rod Dystrophy 24 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Cone-Rod Dystrophy(ID:disease_node_16580) (Disease)