Disease #00063 (MKS4 (Meckel syndrome, type 4), OMIM:611134)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MKS4
Name	Meckel syndrome, type 4
OMIM ID	611134
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CEP290
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-10-17 13:21:33 +02:00 (CEST)
Date last edited	2023-11-30 09:00:12 +01:00 (CET)

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