JSON

cone-rod dystrophy

^ http://purl.obolibrary.org/obo/MONDO_0015993

Inherited retinal dystrophies that belong to the group of pigmentary retinopathies. [ Orphanet:1872 ]

Term info

database cross reference
  • OMIMPS:120970 (MONDO:equivalentTo)
  • Orphanet:1872 (MONDO:equivalentTo)
  • GARD:0010790 (MONDO:equivalentTo)
  • ICD10CM:H35.5 (Orphanet:1872/ntbt)
  • MESH:D000071700 (MONDO:equivalentTo)
  • DOID:0050572 (MONDO:equivalentTo)
Subsets

ordo_disease

abbreviation
CRD [ Orphanet:1872 ]

definition

Inherited retinal dystrophies that belong to the group of pigmentary retinopathies.

exactMatch

http://purl.obolibrary.org/obo/Orphanet_1872, http://purl.obolibrary.org/obo/DOID_0050572, https://omim.org/phenotypicSeries/PS120970, http://identifiers.org/mesh/D000071700

has exact synonym

cone-rod retinal dystrophy, CRD

has related synonym

cone rod dystrophy

id

MONDO:0015993

Term relations