Disease #04398 (HRPT2 (hyperparathyroidism-jaw tumor syndrome, type 2 (HRPT-2)), OMIM:145001)
| Official abbreviation |
HRPT2 |
| Name |
hyperparathyroidism-jaw tumor syndrome, type 2 (HRPT-2) |
| OMIM ID |
145001 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CDC73 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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