Overview
Congenital melanosis is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Congenital melanosis of sclera(child)
Centrofacial lentiginosis syndrome(child)
Hereditary benign acanthosis nigricans with insulin resistance(child)
Peutz-Jeghers syndrome(child)
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome(child)
Familial generalised lentiginosis(child)
Hereditary benign acanthosis nigricans(child)
Acromelanosis(child)
Melanosis oculi(child)
Arterial dissection and lentiginosis syndrome(child)
Dermal melanocytic hamartoma(child)
Melanosis(parent)
Congenital disease(parent)
Quick Facts
- SNOMED CT
- 86042009
- UMLS CUI
- C0221216
- Fully Specified Name
- Congenital melanosis (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.