Disease #00085 (COH-1 (Cohen syndrome (COH-1)), OMIM:216550)

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Official abbreviation	COH-1
Name	Cohen syndrome (COH-1)
OMIM ID	216550
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	VPS13B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-11-16 14:42:10 +01:00 (CET)
Date last edited	N/A