763325000: Insulin resistance (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Disorder of body system\Disorder of endocrine system\Insulin resistance (disorder)

\Metabolic disease\Disorder of carbohydrate metabolism\...

\Disorder of carbohydrate absorption\Malabsorption of glucose\Insulin resistance (disorder)

\Disorder of glucose regulation\Insulin resistance (disorder)

\Disorder of carbohydrate transport\Malabsorption of glucose\Insulin resistance (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3638562017 Insulin resistance (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3638563010 Insulin resistance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Insulin resistance (disorder)	Is a	Disorder of glucose regulation	true	Inferred relationship	Some
Insulin resistance (disorder)	Is a	Malabsorption of glucose	true	Inferred relationship	Some
Insulin resistance (disorder)	Finding site	Structure of endocrine system (body structure)	true	Inferred relationship	Some	1
Insulin resistance (disorder)	Is a	Disorder of endocrine system	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Insulin resistance - type A	Is a	True	Insulin resistance (disorder)	Inferred relationship	Some
Insulin resistance - type B	Is a	True	Insulin resistance (disorder)	Inferred relationship	Some
A rare genetic lipodystrophy with characteristics of loss of subcutaneous adipose tissue primarily affecting the lower limbs and gluteal region due to a defect in the PLIN1 gene. Associated features of insulin resistance, hepatic steatosis, dyslipidemia, hypertension, axillary acanthosis nigricans and muscular hypertrophy of the lower limbs are typical. Caused by heterozygous mutation in the PLIN1 gene on chromosome 15q26.	Is a	True	Insulin resistance (disorder)	Inferred relationship	Some
Leprechaunism syndrome	Is a	True	Insulin resistance (disorder)	Inferred relationship	Some
A rare genetic endocrine disease characterized by intrauterine growth restriction, failure of an adolescent growth spurt with proportional adult short stature, insulin resistance, and early adulthood-onset diabetes. Minimal subluxation of the fifth metacarpal-phalangeal joint has been reported, while metaphyseal dysplasia is absent. Testicular volume is low, but fertility is normal. There is no evidence of primary adrenal insufficiency.	Is a	True	Insulin resistance (disorder)	Inferred relationship	Some
A rare familial partial lipodystrophy characterized by severe partial lipoatrophy affecting the limbs, trunk, and abdomen, together with faciocervical fat accumulation. Additional manifestations include diabetes, acanthosis nigricans, liver steatosis, and hypertriglyceridemia, as well as low serum leptin and adiponectin levels. Severe cardiac rhythm and conduction disturbances have also been reported.	Is a	True	Insulin resistance (disorder)	Inferred relationship	Some
A rare genetic disease characterized by severe pre- and postnatal growth failure with short stature and microcephaly, facial dysmorphism (including a small jaw and prominent midface), severe insulin resistance, fatty liver, and hypertriglyceridemia developing in childhood, and primary gonadal failure. Mild global learning difficulties and acanthosis nigricans have also been reported.	Is a	True	Insulin resistance (disorder)	Inferred relationship	Some
Alstrom syndrome	Is a	True	Insulin resistance (disorder)	Inferred relationship	Some

Reference Sets

Description inactivation indicator reference set