Term Name: | cone-rod dystrophy 2 |
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Synonyms: | cone-rod retinal dystrophy 2, CORD2, CRD2, RCRD2, retinal cone-rod dystrophy 2 |
Definition: | A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13. |
Ontology: | Human Disease [DOID:0111005] ( DOID:0111005 ) |