Disease #00075 (MKS-3 (Meckel syndrome, type 3 (MKS-3)), OMIM:607361)

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	Curator: Johan T. den Dunnen

Official abbreviation	MKS-3
Name	Meckel syndrome, type 3 (MKS-3)
OMIM ID	607361
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TMEM67
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-11-09 15:01:06 +01:00 (CET)
Date last edited	N/A