Disease #00079 (MKS5 (Meckel syndrome, type 5), OMIM:611561)

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	MKS5
Name	Meckel syndrome, type 5
OMIM ID	611561
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RPGRIP1L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-11-09 15:17:02 +01:00 (CET)
Date last edited	2023-11-30 09:00:32 +01:00 (CET)

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