OMOP Concept 4266035
Growth hormone deficiency
StandardConditionSNOMED397827003Disorder
Maps from
3
Descendants
17
Valid from
31 Jul 2003
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Growth hormone deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139240 | Growth hormone deficiency | Non-standard |
| OXMIS | 2531GH | GROWTH HORMONE DEFICIENCY | Non-standard |
| Read | C133.12 | Hypophyseal dwarfism | Non-standard |
Synonyms
Alternative names recorded for Growth hormone deficiency across source vocabularies.
- deficiencia de somatotrofina
- deficiencia de somatotrofina (trastorno)
- GHD - Growth hormone deficiency
- Growth hormone deficiency (disorder)
- Growth hormone insufficiency
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Disorder of anterior pituitary
- 1Hypopituitarism
- 2Disorder of pituitary gland
- 3Disorder of brain
- 3Disorder of endocrine system
- 4Disorder of body system
- 4Disorder of head
- 4Disorder of the central nervous system
- 4Finding of brain
- 5Central nervous system finding
- 5Disease
- 5Disorder of nervous system
- 5Head finding
- 6Clinical finding
Narrower concepts
(17)Included automatically when you query with descendants.
- 1Adult growth hormone deficiency
- 1Growth hormone deficiency after bone marrow transplant
- 1Growth hormone neurosecretory dysfunction
- 1Hereditary growth hormone deficiency
- 1Idiopathic growth hormone deficiency
- 1Isolated somatotropin deficiency
- 1Partial growth hormone deficiency
- 1Psychosocial growth hormone deficiency
- 1Transient somatotropin deficiency
- 2Adult growth hormone deficiency with onset in childhood
- 2Adult-onset growth hormone deficiency
- 2Autosomal dominant isolated somatotropin deficiency
- 2Autosomal recessive isolated somatotropin deficiency
- 2Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
- 2Growth delay due to insulin-like growth factor type 1 deficiency
- 2Immunoglobulinemia with isolated somatotropin deficiency
- 2Nonfamilial hyperinsulinemic isolated somatotropin deficiency
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