Pituitary Dwarfism

Preferred Label : Pituitary Dwarfism;

NCIt definition : Proportionately decreased bodily growth due to failure of the pituitary gland to produce an adequate supply of growth hormone.;

Details

Origin ID

C34555;

UMLS CUI

C0013338;

Automatic exact mappings (from CISMeF team)
- Hypopituitarism [ICD-10 Sub-category (who)]
- Isolated growth hormone deficiency, type ia [OMIM Phenotype]
- Laron syndrome [OMIM Phenotype]
- Nonacquired isolated growth hormone deficiency [ICD-11 More detail]
- Pituitary dwarfism [PASCAL descriptor]
- Pituitary hormone deficiency, combined, 2 [OMIM Phenotype]
Currated CISMeF NLP mapping
- Pituitary dwarfism [ACR pathology]
- Pituitary dwarfism [ACR pathology]
- Pituitary dwarfism [ICD-9 code]
- Pituitary dwarfism [HPO term]
- Pituitary dwarfism [MedDRA LLT]
- dwarfism, pituitary [MeSH Descriptor]
- dwarfism, pituitary [MeSH concept]
- pituitary dwarfism [SNOMED Notion]
DO Cross reference
- isolated growth hormone deficiency [DO Concept]
False automatic mappings
- Pituitary dwarfism (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Non-acquired isolated growth hormone deficiency [ORDO Disease]
- Pituitary dwarfism [ICD-9 code]
- Pituitary dwarfism [MedDRA LLT]
- Pituitary dwarfism [HPO term]
- Pituitary dwarfism [ACR pathology]
- Pituitary dwarfism [ACR pathology]
- Pituitary dwarfism (disorder) [SNOMED CT concept]
- dwarfism, pituitary [MeSH concept]
- dwarfism, pituitary [MeSH Descriptor]
- isolated growth hormone deficiency [DO Concept]
- isolated somatotropin deficiency [SNOMED Notion]
- pituitary dwarfism [SNOMED Notion]
disease_has_associated_gene
- GHR Gene [NCIt concept]
- GHR wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

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