primary hyperparathyroidism

Summary

DOID:11202 - primary hyperparathyroidism

Disease Ontology Definition:A hyperparathyroidism that is characterized by overproduction of parathyroid hormone and elevated levels of calcium in the blood.

Synonyms: familial benign hypercalcemia (disorder), familial primary hyperparathyroidism, primary hyperparathyroidism (disorder)

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010837 - primary hyperparathyroidism

MONDO:0010837 - primary hyperparathyroidism

MIM:

MIM:600166 - HYPERPARATHYROIDISM, PRIMARY, CAUSED BY WATER CLEAR CELL HYPERPLASIA

MIM:600166 - HYPERPARATHYROIDISM, PRIMARY, CAUSED BY WATER CLEAR CELL HYPERPLASIA

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): hyperparathyroidism (is_a)