Congenital muscular dystrophy with arthrogryposis multiplex congenita

disorder

SNOMED 240061000CUI C0410178

Overview

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

Related Conditions

Congenital hereditary muscular dystrophy(parent)

Arthrogryposis multiplex congenita(parent)

Inherited arthrogryposis(parent)

Chronic arthropathy(parent)

Quick Facts

SNOMED CT: 240061000
UMLS CUI: C0410178
Fully Specified Name: Congenital muscular dystrophy with arthrogryposis multiplex congenita (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.