Familial generalised lentiginosis

disorder

SNOMED 765195000CUI C4707357

Overview

Familial generalised lentiginosis is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Autosomal dominant hereditary disorder(parent)

Lentiginosis(parent)

Congenital pigmentary skin anomalies(parent)

Congenital hamartoma of skin(parent)

Congenital melanosis(parent)

Hereditary hypermelanosis(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 765195000
UMLS CUI: C4707357
Fully Specified Name: Familial generalized lentiginosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.