Disease #02546 (HTX-2 (heterotaxy, visceral, autosomal, type 2 (HTX-2, situs ambiguus)), OMIM:605376)

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Official abbreviation	HTX-2
Name	heterotaxy, visceral, autosomal, type 2 (HTX-2, situs ambiguus)
OMIM ID	605376
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CFC1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A