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
|