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familial primary hyperparathyroidism

Disease Summary
Associated Targets (8)
Tbio

5

Tchem

2

Tclin

1


Mondo Description An instance of primary hyperparathyroidism (disease) that is caused by an inherited modification of the individual's genome.
Mondo Term and Equivalent IDs
MONDO:0016365:  familial primary hyperparathyroidism
GARD:0002837: 
Orphanet:2207: 
UMLS:CN201220: