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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