Disease #03249 (COD4;ACHM5 (dystrophy, cone, type 4 (ACHM5)), OMIM:613093)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	COD4;ACHM5
Name	dystrophy, cone, type 4 (ACHM5)
OMIM ID	613093
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PDE6C
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-03-13 09:50:21 +01:00 (CET)

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