Disease #05687 (RP75 (retinitis pigmentosa, type 75 (RP75)), OMIM:617023)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP75
Name	retinitis pigmentosa, type 75 (RP75)
OMIM ID	617023
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	AGBL5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-01-26 21:19:51 +01:00 (CET)
Date last edited	N/A

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