Insulin Resistant Diabetes Mellitus with Acanthosis Nigricans and Hyperandrogenism

Preferred Label : Insulin Resistant Diabetes Mellitus with Acanthosis Nigricans and Hyperandrogenism;

NCIt related terms : Type A Insulin Resistance Syndrome;

Alternative definition : NICHD: A syndrome of insulin resistance caused by mutation(s) in the INSR gene, encoding the insulin receptor. This condition is characterized by a clinical triad of hyperinsulinemia, acanthosis nigricans, and hyperandrogenism without lipodystrophy. This is the least severe of a spectrum of disorders; the other two conditions are Rabson-Mendenhall Syndrome and Donohoe Syndrome.;

Détails

Origin ID

C131836;

UMLS CUI

C0342336;

Currated CISMeF NLP mapping
- Insulin resistance - type A (disorder) [SNOMED CT concept]
- Insulin-resistance syndrome type A [ORDO Disease]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Endocrine Gland [NCIt concept]
- Endocrine System [NCIt concept]
- Pancreas [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Insulin resistance - type A (disorder) [SNOMED CT concept]
- Insulin-resistance syndrome type A [ORDO Disease]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]
disease_has_normal_cell_origin
- Islet Cell [NCIt concept]
disease_has_normal_tissue_origin
- Islet of Langerhans [NCIt concept]
disease_has_primary_anatomic_site
- Digestive System [NCIt concept]
- Endocrine System [NCIt concept]
- Islet of Langerhans [NCIt concept]
- Pancreas [NCIt concept]
disease_mapped_to_gene
- INSR Gene [NCIt concept]

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

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