Disease #07264 (RP101 (retinitis pigmentosa, type 101), OMIM:621548)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	RP101
Name	retinitis pigmentosa, type 101
OMIM ID	621548
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CLN3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-06-27 17:12:21 +02:00 (CEST)
Date last edited	N/A

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.