Preferred Label : Cone rod dystrophy;
ICD-11 definition : Cone rod dystrophies (CRDs) are inherited retinal dystrophies that belong to the group
of pigmentary retinopathies. CRDs are characterized by retinal pigment deposits, visible
on fundus examination, predominantly localized to the macular region. CRD is characterized
by primary cone involvement or, sometimes, by concomitant loss of both cones and rods,
explaining the predominant symptoms of CRDs: decreased visual acuity, color vision
defects, photoaversion and decreased sensitivity in the central visual field, later
followed by progressive loss in peripheral vision and night blindness.;
CISMeF acronym : CRD;
Origin ID : 2109196114;
Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
Cone rod dystrophies (CRDs) are inherited retinal dystrophies that belong to the group
of pigmentary retinopathies. CRDs are characterized by retinal pigment deposits, visible
on fundus examination, predominantly localized to the macular region. CRD is characterized
by primary cone involvement or, sometimes, by concomitant loss of both cones and rods,
explaining the predominant symptoms of CRDs: decreased visual acuity, color vision
defects, photoaversion and decreased sensitivity in the central visual field, later
followed by progressive loss in peripheral vision and night blindness.
