Trichodysplasia xeroderma syndrome

disorder

SNOMED 766812005CUI C4707844

Overview

Trichodysplasia xeroderma syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Brittle hair

Very frequent (80-99%)HP:0002299

Pili torti

Very frequent (80-99%)HP:0003777

Rough hair texture

Very frequent (80-99%)HP:0002208

Sparse eyebrow

Very frequent (80-99%)HP:0045075

Thinning scalp hair

Very frequent (80-99%)HP:0002209

Trichodysplasia

Very frequent (80-99%)HP:0002552

Trichorrhexis nodosa

Very frequent (80-99%)HP:0009886

Xerosis

Very frequent (80-99%)HP:0000958

Hair loss

Frequent (30-79%)HP:0001596

Sparse body hair

Frequent (30-79%)HP:0002231

Related Conditions

Xeroderma(parent)

Autosomal dominant hereditary disorder(parent)

Genetic defect of hair shaft(parent)

Hereditary disorder of the integument(parent)

Developmental hereditary disorder(parent)

Congenital anomaly of hair(parent)

Quick Facts

SNOMED CT: 766812005
UMLS CUI: C4707844
Fully Specified Name: Trichodysplasia xeroderma syndrome (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.