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
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