Disease #00958 (MKS-2 (Meckel syndrome, type 2 (MKS-2)), OMIM:603194)

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Official abbreviation	MKS-2
Name	Meckel syndrome, type 2 (MKS-2)
OMIM ID	603194
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TMEM216
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A