Related Conditions
Self-healing collodion baby(child)
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome(child)
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome(child)
Congenital ichthyosis with hypotrichosis syndrome(child)
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome(child)
Bathing suit ichthyosis(child)
Ichthyosis, oral and digital anomalies syndrome(child)
Congenital cataract ichthyosis syndrome(child)
Passwell Goodman Siprkowski syndrome(child)
Ichthyosis exfoliativa(child)
KLICK syndrome(child)
Ichthyosis linearis circumflexa(child)
Harlequin ichthyosis(child)
Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome(child)
Congenital ichthyosis type 4(child)
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome(child)
Neu-Laxova syndrome(child)
Autosomal recessive keratitis-ichthyosis-deafness syndrome(child)
Autosomal recessive epidermolytic ichthyosis(child)
Hereditary skin peeling syndrome(child)
Quick Facts
- SNOMED CT
- 402772005
- UMLS CUI
- C1274215
- Fully Specified Name
- Autosomal recessive ichthyosis (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.