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Muscle AMP deaminase deficiency

disorder
SNOMED 9105005CUI C0268123

Overview

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

Related Conditions

Hereditary disorder of musculoskeletal system(parent)
Recessive hereditary disorder (autosomal)(parent)
Disorder of purine metabolism(parent)
Metabolic myopathy(parent)
Enzymopathy(parent)

Quick Facts

SNOMED CT
9105005
UMLS CUI
C0268123
Fully Specified Name
Muscle adenosine monophosphate deaminase deficiency (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.