hyperparathyroidism 2 with jaw tumors An 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. GARD:0010829 HPT-JT HRPT2 ICD10:E21.0 MONDO:0007768 NCIT:C48287 OMIM:145001 Orphanet:99880 SCTID:702378002 UMLS:C1704981 familial primary hyperparathyroidism with multiple ossifying jaw fibromas hereditary hyperparathyroidism-jaw tumor syndrome https://rarediseases.info.nih.gov/diseases/10829/hyperparathyroidism-jaw-tumor-syndrome hyperparathyroidism 2 hyperparathyroidism 2 with jaw tumors hyperparathyroidism type 2 hyperparathyroidism, familial primary, with multiple ossifying jaw fibromas hyperparathyroidism-2 hyperparathyroidism-jaw tumor syndrome hyperparathyroidism-jaw tumor syndrome, hereditary parathyroid adenomatosis, familial cystic familial primary hyperparathyroidism inherited renal cancer-predisposing syndrome kidney neoplasm