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

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Official abbreviation	MKS-5
Name	Meckel syndrome, type 5 (MKS-5)
OMIM ID	611561
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
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	N/A