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Hypertrophic mitochondrial cardiomyopathy 472316006 SNOMED CT code SNOMED code 472316006 name Hypertrophic mitochondrial cardiomyopathy status active date introduced 2013-01-31 fully specified name(s) Hypertrophic mitochondrial cardiomyopathy (disorder) synonyms Hypertrophic mitochondrial cardiomyopathy attributes - group1 Due to Mitochondrial cytopathy 240096000 attributes - group2 Associated morphology Hypertrophy 56246009 Finding site Myocardium structure 74281007 parents Mitochondrial cardiomyopathy 472315005 Hypertrophic cardiomyopathy due to disorder 890122001 children Combined oxidative phosphorylation defect type 17 775908005 Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome 717812000 Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome 763280005 Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation 771509001 Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome 718713000 Hypertrophic mitochondrial cardiomyopathy associated with cataracts and lactic acidosis 472318007 Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency 771513008 Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency 771478008 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 QRSL1-related combined oxidative phosphorylation defect 1197430005 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 106063007 301095005 56265001 40172005 472315005 472316006 138875005 404684003 106063007 301095005 56265001 40172005 890122001 472316006 ancestors sorted most to least specific
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