Disease #03475 (HCAD (Hirschsprung disease, cardiac defects, autonomic dysfunction (HCAD)), OMIM:613870)

Official abbreviation HCAD
Name Hirschsprung disease, cardiac defects, autonomic dysfunction (HCAD)
OMIM ID 613870
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease -
Associated with 1 gene ECE1
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

7 entries on 1 page. Showing entries 1 - 7.
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     
00133232 VH108C - - M - Viet Nam - - - - - HCAD - CCDC82 CCDC82, NRG1 2 1 Xuehan Zhuang
00133234 HK9C - - M - Hong Kong - - - - - HCAD - A1BG CYP26A1, TMEM175 2 1 Xuehan Zhuang
00133265 HD09C - - M - Hong Kong - - - - - HCAD - - CCT2, PKD1L2, VASH1 3 1 Xuehan Zhuang
00133266 VH106C - - M - Viet Nam - - - - - HCAD - - ERBB4, NRG1, SEMA3A 3 1 Xuehan Zhuang
00133267 HK164C - - M - Hong Kong - - - - - HCAD - - NRG1, ZEB2 2 1 Xuehan Zhuang
00133268 HK180C - - M - Hong Kong - - - - - HCAD - - DCC 1 1 Xuehan Zhuang
00134081 VH105C - - - - - - - - - - HCAD - - CSMD3 1 1 Xuehan Zhuang
Legend   How to query  


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