Disease #02301 (HHT2 (telangiectasia, hemorrhagic, hereditary, type 2 (HHT2)), OMIM:600376)
| Official abbreviation |
HHT2 |
| Name |
telangiectasia, hemorrhagic, hereditary, type 2 (HHT2) |
| OMIM ID |
600376 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ACVRL1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-01-11 15:44:29 +01:00 (CET) |
Individuals
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