Overview
Familial progressive hyperpigmentation is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Blotchy loss of skin colour
Occasional (5-29%)HP:0001045
Cafe-au-lait spots
HP:0000957
Epidermal hyperkeratosis
HP:0000962
Hyperpigmented macules
HP:0001034
Hypopigmented skin patches
HP:0001053
Multiple lentigines
HP:0001003
Progressive hyperpigmentation
HP:0007505
Quick Facts
- SNOMED CT
- 715630006
- UMLS CUI
- C1840392
- Fully Specified Name
- Familial progressive hyperpigmentation (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 7
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.