Disease #07268 (RP98 (retinitis pigmentosa, type 98), OMIM:620996)

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	RP98
Name	retinitis pigmentosa, type 98
OMIM ID	620996
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TMEM216
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-06-27 17:22:33 +02:00 (CEST)
Date last edited	N/A

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