Insulin-Like growth factor I deficiency

Preferred Label : Insulin-Like growth factor I deficiency;

MeSH note : mutation in IGF1;

MeSH synonym : growth retardation with sensorineural deafness and mental retardation; IGF1 deficiency;

Details

Origin ID

C563867;

UMLS CUI

C1837475;

Automatic exact mappings (from CISMeF team)
- Growth delay due to insulin-like growth factor I deficiency [ICD-11 More detail]
- Insulin Growth Factor I Deficiency [NCIt concept]
Currated CISMeF NLP mapping
- Growth delay due to insulin-like growth factor type 1 deficiency [ORDO Disease]
- Growth delay due to insulin-like growth factor type 1 deficiency (disorder) [SNOMED CT concept]
- Insulin-like growth factor I deficiency [OMIM Phenotype]
MeSH term(s) associated for indexing
- growth disorders [MeSH Descriptor]
- hearing loss, sensorineural [MeSH Descriptor]
- insulin-like growth factor i [MeSH Descriptor]
Record concept(s)
- Insulin-Like growth factor I deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Growth delay due to insulin-like growth factor type 1 deficiency [ORDO Disease]
- Growth delay due to insulin-like growth factor type 1 deficiency (disorder) [SNOMED CT concept]
- Insulin Growth Factor I Deficiency [NCIt concept]
- Insulin-like growth factor I deficiency [OMIM Phenotype]

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