Disease #00166 (HPT-JT (Hyperparathyroidism-Jaw Tumor Syndrome), OMIM:145001)
Official abbreviation |
HPT-JT |
Name |
Hyperparathyroidism-Jaw Tumor Syndrome |
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 |
- |
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