Disease #05702 (RP87 (retinitis pigmentosa, type 87, choroidal involvement (RP87)), OMIM:618697)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP87
Name	retinitis pigmentosa, type 87, choroidal involvement (RP87)
OMIM ID	618697
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RPE65
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-02-26 09:52:51 +01:00 (CET)
Date last edited	2020-02-26 09:55:04 +01:00 (CET)

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