Related Conditions
Cutis laxa, autosomal dominant(child)
Neonatal cutis laxa with marfanoid phenotype(child)
Cutis laxa, x-linked(child)
Cutis laxa, autosomal recessive(child)
Localised congenital cutis laxa(child)
SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome(child)
Cutis laxa(parent)
Congenital connective tissue disorder(parent)
Connective tissue hereditary disorder(parent)
Hereditary disorder of the integument(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 254220005
- UMLS CUI
- C0432334
- Fully Specified Name
- Inherited cutis laxa (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.