Disease #05706 (RP83 (retinitis pigmentosa, type 83 (RP83)), OMIM:618173)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP83
Name	retinitis pigmentosa, type 83 (RP83)
OMIM ID	618173
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ARL3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-02-26 12:18:28 +01:00 (CET)
Date last edited	N/A

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