Familial multiple trichodiscoma

disorder

SNOMED 1222705009CUI C1860850

Overview

Familial multiple trichodiscoma 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.

Abnormality of the hair shaft

HP:0001595

Related Conditions

Autosomal dominant hereditary disorder(parent)

Trichodiscoma(parent)

Hereditary disorder of the integument(parent)

Dermatosis in childhood(parent)

Familial neoplastic disease(parent)

Quick Facts

SNOMED CT: 1222705009
UMLS CUI: C1860850
Fully Specified Name: Familial multiple discoid fibroma (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 1

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.