Alopecia totalis

disorder

SNOMED 19754005CUI C0263504

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.

Absence of scalp hair

Very frequent (80-99%)HP:0002293

Total alopecia

Very frequent (80-99%)HP:0007418

Autoimmune disorder

Occasional (5-29%)HP:0002960

Blotchy loss of skin colour

Occasional (5-29%)HP:0001045

Fragile nails

Occasional (5-29%)HP:0001808

Inflammatory bowel disease

Occasional (5-29%)HP:0002037

Nail pitting

Occasional (5-29%)HP:0001803

Oncholysis

Occasional (5-29%)HP:0001806

Trachyonychia

Occasional (5-29%)HP:0030804

Type I diabetes mellitus

Occasional (5-29%)HP:0100651

Related Conditions

Alopecia antibody deficiency(child)

Alopecia(parent)

Quick Facts

SNOMED CT: 19754005
UMLS CUI: C0263504
Fully Specified Name: Alopecia totalis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.