FAMMM - Familial atypical mole malignant melanoma syndrome

disorder

SNOMED 254819008CUI C0013403

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.

Abnormal eye

HP:0000478

Atypical nevi in non-sun exposed areas

HP:0001074

Atypical nevus

HP:0001062

Cutaneous melanoma

HP:0012056

Intraocular melanoma

HP:0007716

Multiple pigmented nevi

HP:0001054

Related Conditions

Atypical naevus of skin(parent)

Hereditary disorder of the integument(parent)

Hereditary neoplastic syndrome(parent)

Quick Facts

SNOMED CT: 254819008
UMLS CUI: C0013403
Fully Specified Name: Atypical mole syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 6

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.