Disease #00389 (TOF (tetralogy of Fallot (TOF)), OMIM:187500)

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Official abbreviation	TOF
Name	tetralogy of Fallot (TOF)
OMIM ID	187500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 7 genes	GATA4, GATA6, GDF1, JAG1, NKX2-5, TBX1, ZFPM2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-05-30 08:58:25 +02:00 (CEST)
Date last edited	N/A