Disease #02893 (RCD3A;ACHM6 (dystrophy, retinal cone, type 3A (ACHM6)), OMIM:610024)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RCD3A;ACHM6
Name	dystrophy, retinal cone, type 3A (ACHM6)
OMIM ID	610024
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PDE6H
Associated tissues	-
Disease features	autosomal recessive/dominant
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-03-13 09:51:36 +01:00 (CET)

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