Disease #07270 (RP96 (retinitis pigmentosa, type 96), OMIM:620228)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP96
Name	retinitis pigmentosa, type 96
OMIM ID	620228
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SAG
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-06-27 17:24:21 +02:00 (CEST)
Date last edited	N/A

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