Familial progressive hyperpigmentation and hypopigmentation of skin

disorder

SNOMED 763368004CUI C4706423

Overview

Familial progressive hyperpigmentation and hypopigmentation of skin is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Congenital pigmentary skin anomalies(parent)

Genetic disorder of skin pigmentation(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of the integument(parent)

Quick Facts

SNOMED CT: 763368004
UMLS CUI: C4706423
Fully Specified Name: Familial progressive hyperpigmentation and hypopigmentation of skin (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.

Familial progressive hyperpigmentation and hypopigmentation of skin — Symptoms, Testing & Specialists | Ltrl | Healos