Overview
Congenital keratoderma is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Huriez syndrome(child)
Erythrokeratodermia variabilis(child)
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome(child)
Keratoderma hereditarium mutilans with ichthyosis syndrome(child)
Erythrokeratoderma(parent)
Keratoderma(parent)
Congenital disease(parent)
Fetal and/or neonatal disorder of integument(parent)
Quick Facts
- SNOMED CT
- 6874009
- UMLS CUI
- C0265963
- Fully Specified Name
- Congenital 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.