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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000001013
http://purl.bioontology.org/ontology/NDFRT/N0000001013
|
|---|---|
| Preferred Name | Dwarfism, Pituitary [Disease/Finding] |
| Synonyms |
Growth Hormone Deficiency Dwarfism
Isolated Somatotropin Deficiency Disorder
Dwarfism, Pituitary
Hyposomatotrophic Dwarfism
Isolated GH Deficiency
Isolated Growth Hormone Deficiency
Isolated Somatotropin Deficiency
Dwarfism, Growth Hormone Deficiency
Nanism, Pituitary
Isolated HGH Deficiency
Isolated Human Growth Hormone Deficiency
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|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Growth Hormone Deficiency Dwarfism
Isolated Somatotropin Deficiency Disorder
Dwarfism, Pituitary
Hyposomatotrophic Dwarfism
Isolated GH Deficiency
Isolated Growth Hormone Deficiency
Isolated Somatotropin Deficiency
Dwarfism, Growth Hormone Deficiency
Nanism, Pituitary
Isolated HGH Deficiency
Isolated Human Growth Hormone Deficiency
See more
See less
|
|---|---|
| prefLabel | Dwarfism, Pituitary [Disease/Finding]
|
| notation | N0000001013
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| MESH DEFINITION | A form of dwarfism caused by complete or partial GROWTH HORMONE deficiency, resulting from either the lack of GROWTH HORMONE-RELEASING FACTOR from the HYPOTHALAMUS or from the mutations in the growth hormone gene (GH1) in the PITUITARY GLAND. It is also known as Type I pituitary dwarfism. Human hypophysial dwarf is caused by a deficiency of HUMAN GROWTH HORMONE during development.
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| MESH UI | M0006899
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| subClassOf | |
| Semantic type UMLS property | |
| MeSH name | Dwarfism, Pituitary
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| NDFRT kind | DISEASE_KIND
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| type | |
| SNOMED CID | 367460001
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| May be diagnosed by | |
| tui | T047
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| NUI | N0000001013
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| cui | C0013338
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| MESH DUI | D004393
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| Delete | Subject | Author | Type | Created |
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| No notes to display |