Disease #06966 (RP89 (retinitis pigmentosa, type 89), OMIM:618955)

Global Variome shared LOVD

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

Official abbreviation	RP89
Name	retinitis pigmentosa, type 89
OMIM ID	618955
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KIF3B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-09-18 13:49:48 +02:00 (CEST)
Date last edited	2022-09-18 13:50:17 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.