Marie Unna syndrome

disorder

SNOMED 254234005CUI C2931059

Overview

Marie Unna 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.

Hair loss

Very frequent (80-99%)HP:0001596

Partial to total absence of eyelashes

Very frequent (80-99%)HP:0200102

Rough hair texture

Very frequent (80-99%)HP:0002208

Sparse or absent eyebrows

Very frequent (80-99%)HP:0100840

Thinning scalp hair

Very frequent (80-99%)HP:0002209

Related Conditions

Hereditary disorder of the integument(parent)

Congenital hypotrichia(parent)

Autosomal dominant hereditary disorder(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 254234005
UMLS CUI: C2931059
Fully Specified Name: Marie Unna syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.