Chondrodysplasia punctata, X-linked recessive type

disorder

SNOMED 254082007CUI C0432223

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Chondrodysplasia punctata(parent)

X-linked recessive hereditary disease(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of musculoskeletal system(parent)

Quick Facts

SNOMED CT: 254082007
UMLS CUI: C0432223
Fully Specified Name: Chondrodysplasia punctata, X-linked recessive type (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.