- OMIM ID
-
145001
- OMIM term:
- HYPERPARATHYROIDISM 2; HRPT2
- Alternative terms:
-
HYPERPARATHYROIDISM, FAMILIAL PRIMARY, WITH MULTIPLE OSSIFYING JAW FIBROMAS
HYPERPARATHYROIDISM-JAW TUMOR SYNDROME, HEREDITARY; HPT-JT PARATHYROID ADENOMATOSIS, FAMILIAL CYSTIC, INCLUDED
- (∗) Location:
- 1q31.2
- (†) Associated OMIM genes:
- CDC73
- (‡) Associated MGI genes:
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