Insulin receptor disorder type A
GPTKB entity
Statements (16)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
|
| gptkbp:affects |
gptkb:insulin_receptor
|
| gptkbp:associatedWith |
gptkb:acanthosis_nigricans
hyperinsulinemia |
| gptkbp:cause |
insulin resistance
|
| gptkbp:diagnosedBy |
genetic testing
|
| gptkbp:firstDescribed |
1980s
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:mutationAssociatedWith |
gptkb:INSR_gene
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
hyperglycemia
early-onset diabetes |
| gptkbp:treatment |
insulin-sensitizing agents
|
| gptkbp:bfsParent |
gptkb:Rabson-Mendenhall_syndrome
|
| gptkbp:bfsLayer |
8
|
| http://www.w3.org/2000/01/rdf-schema#label |
Insulin receptor disorder type A
|