Hereditary keratoacanthoma

disorder

SNOMED 716774008CUI C5848325

Overview

Hereditary keratoacanthoma 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.

Epidermal hyperkeratosis

Very frequent (80-99%)HP:0000962

Facial angiofibromas

Very frequent (80-99%)HP:0009720

Open skin sore

Very frequent (80-99%)HP:0200042

Papules

Very frequent (80-99%)HP:0200034

Subcutaneous nodule

Very frequent (80-99%)HP:0001482

Papilloma

Frequent (30-79%)HP:0012740

Oncology

Occasional (5-29%)HP:0002664

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of the integument(parent)

Hereditary neoplastic syndrome(parent)

Multiple keratoacanthoma of skin(parent)

Quick Facts

SNOMED CT: 716774008
UMLS CUI: C5848325
Fully Specified Name: Hereditary keratoacanthoma (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

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.