Disease #00149 (JPHT (JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME), OMIM:175050)
| Official abbreviation |
JPHT |
| Name |
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME |
| OMIM ID |
175050 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SMAD4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2023-06-27 09:05:53 +00:00 (UTC) |
| Date last edited |
N/A |
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