Disease #00154 (KNO-2 (Knobloch syndrome, type 2 (KNO-2)), OMIM:608454)

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	Curator: Johan T. den Dunnen

Official abbreviation	KNO-2
Name	Knobloch syndrome, type 2 (KNO-2)
OMIM ID	608454
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ADAMTS18
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-06-20 22:34:06 +02:00 (CEST)
Date last edited	N/A