Overview
Acrokeratosis verruciformis of Hopf 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.
Dystrophic nails
Very frequent (80-99%)HP:0008404
Epidermal hyperkeratosis
Very frequent (80-99%)HP:0000962
Epidermal hyperplasia
Very frequent (80-99%)HP:0025092
Hypergranulosis
Very frequent (80-99%)HP:0025114
Skin-colored papule
Very frequent (80-99%)HP:0025512
Punctate palmoplantar hyperkeratosis
Frequent (30-79%)HP:0007530
Skin plaque
Frequent (30-79%)HP:0200035
Warts
Frequent (30-79%)HP:0200043
White discoloration of nails
Frequent (30-79%)HP:0001820
Anonychia
Occasional (5-29%)HP:0001798
Acantholysis
Excluded (<1%)HP:0100792
Acrokeratosis
HP:0200016
Longitudinal ridging
HP:0001807
Papillomatous papule
HP:0012500
Related Conditions
Inherited disorder of keratinization(parent)
Lesion of skin of foot(parent)
Autosomal dominant hereditary disorder(parent)
Genodermatosis(parent)
Congenital abnormality of hand and digits(parent)
Congenital deformity and malformation of feet and toes(parent)
Disorder of skin of upper limb(parent)
Eruption(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 400085009
- UMLS CUI
- C0265971
- Fully Specified Name
- Acrokeratosis verruciformis of Hopf (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 14
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.