Disease #04397 (HRPT1 (hyperparathyroidism, familial primary, type 1 (HRPT-1)), OMIM:145000)
Official abbreviation |
HRPT1 |
Name |
hyperparathyroidism, familial primary, type 1 (HRPT-1) |
OMIM ID |
145000 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
11 |
Phenotype entries for this disease |
10 |
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) |
Individuals
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