Disease #05878 (RDLKD (dystrophy, retinal, with leukodystrophy (RDLKD)), OMIM:618863)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Mohammed A.M Derar

Official abbreviation	RDLKD
Name	dystrophy, retinal, with leukodystrophy (RDLKD)
OMIM ID	618863
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ACBD5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-11-11 14:50:15 +01:00 (CET)
Date last edited	N/A

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