Disease #06889 (CHTD8 (heart defects, congenital, multiple types, 8, with/without heterotaxy), OMIM:619657)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	CHTD8
Name	heart defects, congenital, multiple types, 8, with/without heterotaxy
OMIM ID	619657
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SMAD2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-01-01 12:59:12 +01:00 (CET)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.