Disease #02318 (RP17 (retinitis pigmentosa, type 17 (RP17)), OMIM:600852)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP17
Name	retinitis pigmentosa, type 17 (RP17)
OMIM ID	600852
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	1
Associated with 3 genes	GDPD1, SMG8, YPEL2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2023-11-06 16:13:11 +01:00 (CET)

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