Insulin resistance - type A

disorder

SNOMED 237651005CUI C0342336

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Delayed puberty

Very frequent (80-99%)HP:0000823

Early bone maturation

Very frequent (80-99%)HP:0005616

Epidermal hyperkeratosis

Very frequent (80-99%)HP:0000962

Generalised hyperpigmentation

Very frequent (80-99%)HP:0007440

Generalized hirsutism

Very frequent (80-99%)HP:0002230

NIDDM

Very frequent (80-99%)HP:0005978

Subcutaneous nodule

Very frequent (80-99%)HP:0001482

Related Conditions

Diabetes mellitus due to genetic defect in insulin action(parent)

Autosomal hereditary disorder(parent)

Insulin resistance(parent)

Hereditary disorder of endocrine system(parent)

Quick Facts

SNOMED CT: 237651005
UMLS CUI: C0342336
Fully Specified Name: Insulin resistance - type A (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.