Disease #05057 (KOS (Kaufman oculocerebrofacial syndrome (KOS)), OMIM:244450)

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	Curator: Johan T. den Dunnen

Official abbreviation	KOS
Name	Kaufman oculocerebrofacial syndrome (KOS)
OMIM ID	244450
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	UBE3B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 11:00:40 +02:00 (CEST)
Date last edited	N/A