Disease #03671 (CORD16;RP64 (dystrophy, cone-rod, type 16 (CORD16), retinitis pigmentosa, type 64 (RP64)), OMIM:614500)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CORD16;RP64
Name	dystrophy, cone-rod, type 16 (CORD16), retinitis pigmentosa, type 64 (RP64)
OMIM ID	614500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	C8orf37
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-08-30 11:04:14 +02:00 (CEST)

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