Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation 771509001
SNOMED CT code
| SNOMED code | 771509001 |
|---|---|
| name | Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation (disorder) |
| synonyms |
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| attributes - group1 | |
| Finding site | Myocardium structure 74281007 |
| Associated morphology | Hypertrophy 56246009 |
| attributes - group4 | |
| Due to | Mitochondrial cytopathy 240096000 |
| attributes - group2 | |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group3 | |
| Finding site | Kidney structure 64033007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Mitochondrial myopathy 16851005 Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation 771509001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Renal tubular acidosis 1776003 Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation 771509001 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Cardiac finding 301095005 Heart disease 56265001 Cardiac complication 40172005 Mitochondrial cardiomyopathy 472315005 Hypertrophic mitochondrial cardiomyopathy 472316006 Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation 771509001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of the genitourinary system 42030000 Disorder of the urinary system 128606002 Urinary complication 49698005 Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation 771509001 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Secondary myopathy 60738003 Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation 771509001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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