Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency

disorder

SNOMED 771513008CUI C4749946

Overview

Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Hypertrophic mitochondrial cardiomyopathy(parent)

Cardiovascular system hereditary disorder(parent)

Mitochondrial cytopathy(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 771513008
UMLS CUI: C4749946
Fully Specified Name: Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 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.