Disease #05522 (HHT1 (telangiectasia hemorrhagic, hereditary, type 1 (HHT1, Osler-Rendu-Weber disease)), OMIM:187300)

Official abbreviation HHT1
Name telangiectasia hemorrhagic, hereditary, type 1 (HHT1, Osler-Rendu-Weber disease)
OMIM ID 187300
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene ENG
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2018-11-23 16:28:57 +01:00 (CET)
Date last edited 2021-01-11 15:46:16 +01:00 (CET)


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     
00229539 - - - - - - - - - - - HHT1 - ENG ENG 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00417648 - - - - - - - - - - - HHT1 - ACVRL1 ACVRL1 1 1 Beatrice Alessandrini
Legend   How to query  


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