Disease #01192 (AOVD1 (aortic valve disease, type 1 (AOVD-1)), OMIM:109730)

Official abbreviation AOVD1
Name aortic valve disease, type 1 (AOVD-1)
OMIM ID 109730
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene NOTCH1
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

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00063402 - PubMed: Bonachea 2014 - - - - - - - - - AOVD1 - PTCH1 PTCH1 1 1 Michel van Geel
00266712 - PubMed: Costa 2013 - - - - - - - - - AOVD1, ASD, CHNG5, coarctation, HLHS1, VSD - NKX2-5 NKX2-5 1 1 Liliana Dain
00266720 - PubMed: Dentice 2006 - - - - - - - - - AOVD1, ASD, CHNG5, coarctation, HLHS1, VSD - NKX2-5 NKX2-5 1 1 Liliana Dain
00266846 - PubMed: Qu 2014 - - - - - - - - - aortic stenosis, AOVD1, ASD7, ATFB - NKX2-5 NKX2-5 1 1 Liliana Dain
00266948 - PubMed: Reamon-Buettner 2013 - - - - - - - - - AOVD1, ASD, CHNG5, coarctation, HLHS1, VSD - NKX2-5 NKX2-5 1 1 Liliana Dain
00266974 - PubMed: van Engelen 2012 - - - - - - - - - AOVD1, ASD, CHNG5, coarctation, HLHS1, VSD - NKX2-5 NKX2-5 1 1 Liliana Dain
Legend   How to query  


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