Disease #04083 (CHTD4 (heart defects, congenital, multiple types, type 4 (CHTD-4)), OMIM:615779)

Official abbreviation CHTD4
Name heart defects, congenital, multiple types, type 4 (CHTD-4)
OMIM ID 615779
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene NR2F2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00029036 MC131 PubMed: El Malti 2016, Journal: El Malti 2016 - M no France European >57y - yes implantable cardiac defibrillator CHTD4, CMD1A congestive heart failure, secundum atrial septal defect third degree atrioventricular block cataract pectus excavatum - NKX2-5 1 1 Patrice Bouvagnet
00032449 - - - F no - European >14y - yes - CHTD4 Bicuspid aortic valve Aorctic coarctation CLTCL1, HIC2, LZTR1, USP18 - 1 1 Patrice Bouvagnet
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