hyperparathyroidism 2

Preferred Label : hyperparathyroidism 2;

MeSH synonym : hyperparathyroidism, familial primary, with multiple ossifying jaw fibromas; Hyperparathyroidism-Jaw tumor syndrome, hereditary; Hpt-Jt; Familial Cystic Parathyroid Adenomatosis; Familial Primary Hyperparathyroidism with Multiple Ossifying Jaw Fibromas; Hereditary Hyperparathyroidism-Jaw Tumor Syndrome; Hyperparathyroidism-Jaw Tumor Syndrome;

Details

Origin ID

C563273;

UMLS CUI

C1704981;

Automatic exact mappings (from CISMeF team)
- CDC73 wt Allele [NCIt concept]
Currated CISMeF NLP mapping
- Hyperparathyroidism - jaw tumour syndrome [ICD-11 More detail]
- Hyperparathyroidism 2 with jaw tumors [OMIM Phenotype]
- Hyperparathyroidism-Jaw Tumor Syndrome [NCIt concept]
- Hyperparathyroidism-jaw tumor syndrome [ORDO Disease]
- Hyperparathyroidism-jaw tumor syndrome (disorder) [SNOMED CT concept]
- hyperparathyroidism jaw tumor syndrome [Disease (Nov.)]
MeSH term(s) associated for indexing
- adenoma [MeSH Descriptor]
- fibroma [MeSH Descriptor]
- hyperparathyroidism [MeSH Descriptor]
- jaw neoplasms [MeSH Descriptor]
Record concept(s)
- hyperparathyroidism 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperparathyroidism 2 with jaw tumors [OMIM Phenotype]
- Hyperparathyroidism-Jaw Tumor Syndrome [NCIt concept]
- Hyperparathyroidism-jaw tumor syndrome [ORDO Disease]
- Hyperparathyroidism-jaw tumor syndrome [MedDRA LLT]
- Hyperparathyroidism-jaw tumor syndrome (disorder) [SNOMED CT concept]
- Hyperparathyroidism-jaw tumour syndrome [MedDRA LLT]
- hyperparathyroidism jaw tumor syndrome [Disease (Nov.)]

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