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Familial multiple trichoepitheliomata

disorder
SNOMED 403825008CUI C1275122

Overview

Familial multiple trichoepitheliomata 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.

Multiple, subcutaneous nodules
Very frequent (80-99%)HP:0001482
Papules
Very frequent (80-99%)HP:0200034
Teleangiectasia of the skin
Frequent (30-79%)HP:0100585
Basal cell nevus
Occasional (5-29%)HP:0002671

Related Conditions

Quick Facts

SNOMED CT
403825008
UMLS CUI
C1275122
Fully Specified Name
Familial multiple trichoepitheliomata (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
4
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.