Hereditary hypotrichosis simplex of scalp

disorder

SNOMED 717256009CUI C1840299

Overview

Hereditary hypotrichosis simplex of scalp 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.

Fine hair

Very frequent (80-99%)HP:0002213

Slow-growing scalp hair

Very frequent (80-99%)HP:0100038

Absence of scalp hair

Frequent (30-79%)HP:0002293

Epidermal hyperkeratosis

Frequent (30-79%)HP:0000962

Parakeratosis

Frequent (30-79%)HP:0001036

Thickening of upper layer of skin

Frequent (30-79%)HP:0025092

Thinning scalp hair

Frequent (30-79%)HP:0002209

Hay fever

Occasional (5-29%)HP:0003193

High immunoglobulin E

Occasional (5-29%)HP:0003212

Prurigo Besnier

Occasional (5-29%)HP:0001047

Scaling skin

Occasional (5-29%)HP:0040189

Skin itching

Occasional (5-29%)HP:0000989

Dental anomalies

Excluded (<1%)HP:0000164

Nail disease

Excluded (<1%)HP:0001597

Related Conditions

Autosomal dominant hereditary disorder(parent)

Disorder of scalp(parent)

Disorder of skin of head(parent)

Hereditary hypotrichosis simplex(parent)

Quick Facts

SNOMED CT: 717256009
UMLS CUI: C1840299
Fully Specified Name: Hereditary hypotrichosis simplex of scalp (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.