Disease #07267 (RP99 (retinitis pigmentosa, type 99), OMIM:301148)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP99
Name	retinitis pigmentosa, type 99
OMIM ID	301148
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IDH3G
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-06-27 17:21:17 +02:00 (CEST)
Date last edited	N/A

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