Disease #00421 (CORD-3 (dystrophy, cone rod, type 3 (CORD-3)), OMIM:604116)

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Official abbreviation	CORD-3
Name	dystrophy, cone rod, type 3 (CORD-3)
OMIM ID	604116
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ABCA4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-06-16 23:03:53 +02:00 (CEST)
Date last edited	N/A