Combined molybdoflavoprotein enzyme deficiency

disorder

SNOMED 29692004CUI C0268119

Overview

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

Related Conditions

Molybdenum cofactor deficiency complementation group C(child)

Molybdenum cofactor deficiency complementation group A(child)

Molybdenum cofactor deficiency complementation group B(child)

Hereditary xanthinuria(parent)

Quick Facts

SNOMED CT: 29692004
UMLS CUI: C0268119
Fully Specified Name: Combined molybdoflavoprotein enzyme 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.