growth factors, combined defect of

Preferred Label : growth factors, combined defect of;

MeSH synonym : insulin, Insulin-Like growth factor I, and epidermal growth factor deficiency; Werner-Like syndrome due to combined growth factor deficiency; Hoepffner dreyer reimers syndrome; Peptide growth factors deficiency; Peptidic growth factors deficiency;

Détails

Origin ID

C565529;

UMLS CUI

C2931279;

Automatic exact mappings (from CISMeF team)
- Lipodystrophy due to peptidic growth factors deficiency [ICD-11 More detail]
- Lipodystrophy due to peptidic growth factors deficiency (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Growth factors, combined defect of [OMIM Phenotype]
- Lipodystrophy due to peptidic growth factors deficiency [ORDO Disease]
MeSH term(s) associated for indexing
- epidermal growth factor [MeSH Descriptor]
- insulin [MeSH Descriptor]
- insulin-like growth factor i [MeSH Descriptor]
- metabolism, inborn errors [MeSH Descriptor]
Record concept(s)
- growth factors, combined defect of [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Growth factors, combined defect of [OMIM Phenotype]
- Lipodystrophy due to peptidic growth factors deficiency [ORDO Disease]
- Lipodystrophy due to peptidic growth factors deficiency (disorder) [SNOMED CT concept]

Position du mot-clé dans l'(les) arborescence(s) :

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