Disease #01048 (VCFS (velocardiofacial syndrome), OMIM:192430)

Official abbreviation VCFS
Name velocardiofacial syndrome
OMIM ID 192430
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 5 genes DGCR14, DGCR2, DGCR6, DGCR8, TBX1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2025-08-26 16:48:45 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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     
00285600 - PubMed: Zweier 2007, PubMed: Fung 2015, PubMed: McDonald-McGinn 1993 - - - - - - - - - VCFS - TBX1 TBX1 1 1 Global Variome, with Curator vacancy
00285610 - PubMed: Gong 2001 - - - - - - - - - VCFS - TBX1 TBX1 1 1 Global Variome, with Curator vacancy
Legend   How to query  


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