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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000001641
http://purl.bioontology.org/ontology/NDFRT/N0000001641
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|---|---|
| Preferred Name | Hypoparathyroidism [Disease/Finding] |
| Synonyms |
Hypoparathyroidism
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | Hypoparathyroidism
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|---|---|
| prefLabel | Hypoparathyroidism [Disease/Finding]
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| MESH DEFINITION | A condition caused by a deficiency of PARATHYROID HORMONE (or PTH). It is characterized by HYPOCALCEMIA and hyperphosphatemia. Hypocalcemia leads to TETANY. The acquired form is due to removal or injuries to the PARATHYROID GLANDS. The congenital form is due to mutations of genes, such as TBX1; (see DIGEORGE SYNDROME); CASR encoding CALCIUM-SENSING RECEPTOR; or PTH encoding parathyroid hormone.
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| MESH DUI | D007011
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| MESH UI | M0010912
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| MeSH name | Hypoparathyroidism
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| type | |
| tui | T047
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| SNOMED CID | 36976004
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| May be treated by |
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| notation | N0000001641
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| Semantic type UMLS property | |
| NUI | N0000001641
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| cui | C0020626
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| NDFRT kind | DISEASE_KIND
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| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |