Preferred Name

Hypoparathyroidism [Disease/Finding]
Synonyms

Hypoparathyroidism

ID

http://purl.bioontology.org/ontology/NDFRT/N0000001641

altLabel

Hypoparathyroidism

cui

C0020626

May be treated by

http://purl.bioontology.org/ontology/NDFRT/N0000177283

http://purl.bioontology.org/ontology/NDFRT/N0000191605

http://purl.bioontology.org/ontology/NDFRT/N0000186740

http://purl.bioontology.org/ontology/NDFRT/N0000177285

http://purl.bioontology.org/ontology/NDFRT/N0000191602

http://purl.bioontology.org/ontology/NDFRT/N0000190451

http://purl.bioontology.org/ontology/NDFRT/N0000192194

http://purl.bioontology.org/ontology/NDFRT/N0000191603

http://purl.bioontology.org/ontology/NDFRT/N0000164474

http://purl.bioontology.org/ontology/NDFRT/N0000188967

http://purl.bioontology.org/ontology/NDFRT/N0000181636

http://purl.bioontology.org/ontology/NDFRT/N0000186739

http://purl.bioontology.org/ontology/NDFRT/N0000192540

http://purl.bioontology.org/ontology/NDFRT/N0000146043

http://purl.bioontology.org/ontology/NDFRT/N0000193750

http://purl.bioontology.org/ontology/NDFRT/N0000177284

http://purl.bioontology.org/ontology/NDFRT/N0000191604

http://purl.bioontology.org/ontology/NDFRT/N0000164680

http://purl.bioontology.org/ontology/NDFRT/N0000152280

http://purl.bioontology.org/ontology/NDFRT/N0000191580

http://purl.bioontology.org/ontology/NDFRT/N0000177282

http://purl.bioontology.org/ontology/NDFRT/N0000146009

http://purl.bioontology.org/ontology/NDFRT/N0000190914

http://purl.bioontology.org/ontology/NDFRT/N0000184477

http://purl.bioontology.org/ontology/NDFRT/N0000190953

http://purl.bioontology.org/ontology/NDFRT/N0000191456

http://purl.bioontology.org/ontology/NDFRT/N0000191550

http://purl.bioontology.org/ontology/NDFRT/N0000192541

http://purl.bioontology.org/ontology/NDFRT/N0000146836

http://purl.bioontology.org/ontology/NDFRT/N0000158433

http://purl.bioontology.org/ontology/NDFRT/N0000192062

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.

MESH DUI

D007011

MeSH name

Hypoparathyroidism

MESH UI

M0010912

NDFRT kind

DISEASE_KIND

notation

N0000001641

NUI

N0000001641

prefLabel

Hypoparathyroidism [Disease/Finding]

SNOMED CID

36976004

tui

T047

subClassOf

http://purl.bioontology.org/ontology/NDFRT/N0000002321

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