a rare inherited condition in which one or more tumors form in the parathyroid glands (four pea-sized organs found on the thyroid) and cause them to make too much parathyroid hormone. the increased parathyroid hormone causes a loss of calcium from the bones and too much calcium in the blood. also called familial isolated hyperparathyroidism.
| human | 遺伝子名 | FIHP |
| 同義語(エイリアス) | hyperparathyroidism 1; HRPT1 | |
| SWISS-PROTのID | --- | |
| EntrezGeneのID | EntrezGene:3278 | |
| その他のDBのID | HGNC:5190 |
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