Disease #05820 (SCAD (artery dissection, coronary, spontaneous (SCAD)), OMIM:122455)

Official abbreviation SCAD
Name artery dissection, coronary, spontaneous (SCAD)
OMIM ID 122455
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease -
Associated with 1 gene COL3A1
Associated tissues -
Disease features -
Remarks -
Date created 2020-08-25 15:23:23 +02:00 (CEST)
Date last edited 2020-08-26 12:18:33 +02:00 (CEST)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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     
00318331 - PubMed: Kaadan et al., 2018 - - - - - - - - - EDS, EDSVASC, SCAD - COL3A1 COL3A1 1 1 Raymond Dalgleish
00318352 - PubMed: Ohyama et al., 2011 The paper cited the substituted amino acid using only legacy numbering. - - - - - - - - EDS, EDSVASC, SCAD - COL3A1 COL3A1 1 1 Raymond Dalgleish
00318765 - PubMed: Kaadan et al., 2018 - - - - - - - - - EDS, EDSVASC, SCAD - COL3A1 COL3A1 1 1 Raymond Dalgleish
00318899 - PubMed: Kaadan et al., 2018 - - - - - - - - - EDS, EDSVASC, SCAD - COL3A1 COL3A1 1 1 Raymond Dalgleish
00319092 - PubMed: Kaadan et al., 2018 - - - - - - - - - SCAD - COL3A1 COL3A1 1 1 Raymond Dalgleish
Legend   How to query  


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