Disease #00395 (ARMD1 (macular degeneration, age-related, type 1 (ARMD-1)), OMIM:603075)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	ARMD1
Name	macular degeneration, age-related, type 1 (ARMD-1)
OMIM ID	603075
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 5 genes	APOE, CFHR1, CFHR3, HMCN1, PLEKHA1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-06-02 08:48:10 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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