Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	CONE-ROD DYSTROPHY 2
Synonyms	CRD
ID	http://purl.bioontology.org/ontology/OMIM/120970
altLabel	CRD CRD2 CORD2 CONE-ROD RETINAL DYSTROPHY RETINAL CONE-ROD DYSTROPHY CONE-ROD DYSTROPHY CORD RCRD2
cui	C0035334
Gene Locus	19q13.3
Gene Symbol	CRD CORD2 CRX LCA7
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	120970
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	CONE-ROD DYSTROPHY 2
tui	T047

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_0111005	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/MESH/D012174	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/ICD10CM/H35.52	International Classification of Diseases, Version 10 - Clinical Modification	CUI