Ulerythema ophryogenes

disorder

SNOMED 400126005CUI C5700076

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.

Blushing

Very frequent (80-99%)HP:0001041

Hyperkeratosis follicularis

Very frequent (80-99%)HP:0007502

Hyperkeratotic papule

Very frequent (80-99%)HP:0045059

Keratosis pilaris

Very frequent (80-99%)HP:0032152

Laterally sparse eyebrows

Very frequent (80-99%)HP:0005338

Red-blue papule

Very frequent (80-99%)HP:0030350

Abnormal forehead morphology

Frequent (30-79%)HP:0000290

Abnormality of the cheek

Frequent (30-79%)HP:0004426

Abnormality of the chin

Frequent (30-79%)HP:0000306

Dry skin

Frequent (30-79%)HP:0000958

Skin degeneration

Frequent (30-79%)HP:0004334

Breaking out

Occasional (5-29%)HP:0001061

Contact dermatitis

Occasional (5-29%)HP:0032282

Related Conditions

Ulerythema of cheeks(child)

Keratosis pilaris atrophicans(parent)

Eruption(parent)

Disorder of hair growth(parent)

Disorder of face(parent)

Disorder of ocular adnexa(parent)

Quick Facts

SNOMED CT: 400126005
UMLS CUI: C5700076
Fully Specified Name: Ulerythema ophryogenes (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.