Overview
Inherited disorder of keratinization is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Erythrokeratoderma(child)
Hereditary erythrokeratolysis(child)
Hereditary follicular keratoses(child)
Bart-Pumphrey syndrome(child)
Familial benign pemphigus(child)
Hereditary acantholytic dermatosis(child)
Acrokeratosis verruciformis of Hopf(child)
Atrophoderma vermiculatum(child)
Congenital ichthyosis of skin(child)
Lelis syndrome(child)
Disseminated superficial porokeratosis(child)
Porokeratosis plantaris palmaris et disseminata(child)
Skin fragillity, woolly hair, palmoplantar keratoderma syndrome(child)
Focal palmoplantar keratoderma with joint keratoses(child)
Diffuse palmoplantar keratoderma with painful fissures(child)
Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering(child)
Leukoencephalopathy, palmoplantar keratoderma syndrome(child)
Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome(child)
Palmoplantar keratoderma, spastic paralysis syndrome(child)
Cutis gyrata syndrome of Beare and Stevenson(child)
Quick Facts
- SNOMED CT
- 254214009
- UMLS CUI
- C0474892
- Fully Specified Name
- Inherited disorder of keratinization (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.