Overview
Inherited cutaneous hyperpigmentation is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Dyschromatosis universalis(child)
Naegeli-Franceschetti-Jadassohn syndrome(child)
Symmetrical dyschromatosis of extremities(child)
DPR - Dermatopathia pigmentosa reticularis(child)
Acromelanosis(child)
Terminal osseous dysplasia and pigmentary defect syndrome(child)
Thumb deformity, alopecia, pigmentation anomaly syndrome(child)
Char Douglas Dungan syndrome(child)
Osteopathia striata, pigmentary dermopathy, white forelock syndrome(child)
Hereditary benign acanthosis nigricans(child)
Hereditary benign acanthosis nigricans with insulin resistance(child)
Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome(child)
Genodermatosis(parent)
Hyperpigmentation of skin(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
- 239079007
- UMLS CUI
- C0406771
- Fully Specified Name
- Inherited cutaneous hyperpigmentation (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.