laron syndrome type 2

Preferred Label : laron syndrome type 2;

MeSH synonym : laron type dwarfism 2; laron syndrome due to postreceptor defect; growth hormone insensitivity due to postreceptor defect; growth hormone insensitivity with immunodeficiency;

Détails

Origin ID

C537871;

UMLS CUI

C1855548;

Currated CISMeF NLP mapping
- Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessive [OMIM Phenotype]
- Laron syndrome with immunodeficiency [ORDO Disease]
- Laron syndrome with immunodeficiency [ICD-11 More detail]
- Laron syndrome with immunodeficiency (disorder) [SNOMED CT concept]
MeSH indexing information
- stat5 transcription factor [MeSH Descriptor]
MeSH term(s) associated for indexing
- laron syndrome [MeSH Descriptor]
Record concept(s)
- Laron syndrome type 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessive [OMIM Phenotype]
- Laron syndrome with immunodeficiency [ORDO Disease]

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

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