Hereditary hypotrichosis simplex

disorder

SNOMED 723362004CUI C1854310

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.

Hair loss

Very frequent (80-99%)HP:0001596

Sparse body hair

Very frequent (80-99%)HP:0002231

Sparse eyebrow

Very frequent (80-99%)HP:0045075

Thin eyelashes

Very frequent (80-99%)HP:0000653

Thinning scalp hair

Very frequent (80-99%)HP:0002209

Thin, sparse hair

Frequent (30-79%)HP:0008070

Decreased sexual hair

HP:0002225

Dental problems

Excluded (<1%)HP:0000164

Dermatopathy

Excluded (<1%)HP:0000951

Nail disease

Excluded (<1%)HP:0001597

sparse to absent axillary hair

HP:0002215

Related Conditions

Hereditary hypotrichosis simplex of scalp(child)

Autosomal hereditary disorder(parent)

Hypotrichosis(parent)

Hereditary disorder of the integument(parent)

Quick Facts

SNOMED CT: 723362004
UMLS CUI: C1854310
Fully Specified Name: Hereditary hypotrichosis simplex (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 11

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.