Overview
Hereditary palmoplantar keratoderma is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Congenital palmoplantar and perioral keratoderma of Olmsted(child)
Mutilating keratoderma(child)
Circumscribed palmoplantar keratoderma(child)
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf(child)
Hereditary diffuse palmoplantar keratoderma(child)
Punctate palmoplantar keratoderma(child)
Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu(child)
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome(child)
Autosomal dominant palmoplantar keratoderma and congenital alopecia(child)
Naxos disease(child)
Woolly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome(child)
Palmoplantar keratoderma with deafness syndrome(child)
Fitzsimmons McLachlan Gilbert syndrome(child)
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome(child)
Wooly hair with palmoplantar keratoderma syndrome(child)
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome(child)
Focal palmoplantar keratoderma with joint keratoses(child)
Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering(child)
Hidrotic ectodermal dysplasia syndrome(child)
Ankylosing vertebral hyperostosis with tylosis syndrome(child)
Quick Facts
- SNOMED CT
- 239066003
- UMLS CUI
- C0406757
- Fully Specified Name
- Hereditary palmoplantar keratoderma (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.