Insulin Growth Factor I Resistance

Preferred Label : Insulin Growth Factor I Resistance;

NCIt related terms : IGF-I Resistance; IGF1R; Somatomedin-C Resistance;

NCIt definition : Tissue unresponsiveness to insulin-like growth factor-I.;

Alternative definition : NICHD: Growth hormone insensitivity/resistance caused by loss-of-function mutation(s) in the IGF1R gene, encoding insulin-like growth factor 1 receptor. This phenotypically variable condition is characterized by clinical features similar to insulin-like growth factor I (IGF-I) deficiency accompanied by increased serum concentrations of IGF-I.;

Détails

Origin ID

C120107;

UMLS CUI

C1849157;

Automatic exact mappings (from CISMeF team)
- Growth delay due to insulin-like growth factor I resistance (disorder) [SNOMED CT concept]
- Insulin-Like growth factor I, resistance to [MeSH Supplementary Concept]
- Insulin-like growth factor I receptor [OMIM gene]
- Insulin-like growth factor I, resistance to [OMIM Phenotype]
- insulin like growth factor 1 receptor [ORDO Gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Growth delay due to insulin-like growth factor I resistance [ORDO Disease]
- Growth delay due to insulin-like growth factor I resistance (disorder) [SNOMED CT concept]
- Insulin-Like growth factor I, resistance to [MeSH Supplementary Concept]
- Insulin-Like growth factor I, resistance to [MeSH concept]
- Insulin-like growth factor I, resistance to [OMIM Phenotype]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]

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

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