Keratosis pilaris atrophicans

disorder

SNOMED 400059005CUI C0263428

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.

Comedo

Always present (100%)HP:0025249

Erythema

Always present (100%)HP:0010783

Failure of development of eyelashes

Always present (100%)HP:0000561

Keratosis pilaris

Always present (100%)HP:0032152

Papules

Always present (100%)HP:0200034

Sparse eyebrow

Always present (100%)HP:0045075

Abnormal perifollicular morphology

HP:0031285

Abnormality of vision

Excluded (<1%)HP:0000504

Dull intelligence

Excluded (<1%)HP:0001249

Increased lacrimation

HP:0009926

Related Conditions

Keratosis follicularis spinulosa decalvans(child)

Atrophoderma vermiculatum(child)

Ulerythema ophryogenes(child)

Keratosis pilaris(parent)

Quick Facts

SNOMED CT: 400059005
UMLS CUI: C0263428
Fully Specified Name: Keratosis pilaris atrophicans (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.