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.

Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency — Symptoms, Testing & Specialists | Ltrl | Ltrl