Disease #01600 (VRCP;MRCS2 (vitreoretinochoroidopathy (VRCP, MRCS2 included)), OMIM:193220)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	VRCP;MRCS2
Name	vitreoretinochoroidopathy (VRCP, MRCS2 included)
OMIM ID	193220
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	BEST1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-04-30 09:05:14 +02:00 (CEST)

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