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Hyperparathyroidism 2 with jaw tumors
rareAn autosomal dominant inherited syndrome characterized by the development of parathyroid adenoma or carcinoma, ossifying fibroma of the mandible and maxilla, renal neoplasms, and renal cysts.
- Identifiers
- MONDO:0007768 OMIM:145001Orphanet:99880
- Part of
- Abnormal mineralization disorderBone neoplasmFamilial primary hyperparathyroidismHereditary disorder of connective tissueHereditary neoplastic syndrome
- Also known as
- familial primary hyperparathyroidism with multiple ossifying jaw fibromas · hereditary hyperparathyroidism-jaw tumor syndrome · hereditary hyperparathyroidism-jaw tumour syndrome · HPT-JT · HRPT2
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