Term Name: cone-rod dystrophy 2
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 )

Relationships
is a type of: cone-rod dystrophy
disjoint_from: X-linked cone-rod dystrophy 2