Disease #00071 (MKS9 (Meckel syndrome, type 9 (MKS-9)), OMIM:614209)

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	MKS9
Name	Meckel syndrome, type 9 (MKS-9)
OMIM ID	614209
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	B9D1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-11-09 13:56:55 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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