Disease #03451 (RP48 (retinitis pigmentosa, type 48 (RP48)), OMIM:613827)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	RP48
Name	retinitis pigmentosa, type 48 (RP48)
OMIM ID	613827
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GUCA1B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-04-09 15:05:56 +02:00 (CEST)

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