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763325000: 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
920301000195117 resistenza insulinica it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
821321000241114 résistance à l'insuline fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
821341000241118 insulinorésistance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
868671000195119 Insulinresistenz de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


8 descendants. Search Descendants:

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 characterized by 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. 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

This concept is not in any reference sets

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