Disease #01046 (CTHM (heart malformations,conotruncal (CTHM)), OMIM:217095)

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	Curator: Johan T. den Dunnen

Official abbreviation	CTHM
Name	heart malformations,conotruncal (CTHM)
OMIM ID	217095
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 6 genes	CFC1, GATA6, GDF1, NKX2-5, NKX2-6, TBX1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A