Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008
SNOMED CT code
| SNOMED code | 1186718008 |
|---|---|
| name | Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome |
| status | active |
| date introduced | 2021-11-30 |
| fully specified name(s) | Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome (disorder) |
| synonyms |
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| attributes - group5 | |
| Due to | Mitochondrial cytopathy 240096000 |
| attributes - group4 | |
| Finding site | Nerve structure 3057000 |
| attributes - group2 | |
| Occurrence | Neonatal 255407002 |
| Finding site | Brain structure 12738006 |
| attributes - group3 | |
| Occurrence | Neonatal 255407002 |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group1 | |
| Finding site | Myocardium structure 74281007 |
| Associated morphology | Hypertrophy 56246009 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Neuropathy 386033004 Metabolic neuropathy 1153623003 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of neonate 118188004 Neonatal disease 22925008 Neonatal cardiovascular disorder 363696006 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Mitochondrial encephalomyopathy 447292006 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 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 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Secondary myopathy 60738003 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Specific enzyme deficiency 129456006 Coenzyme Q10 deficiency 724575009 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of neonate 118188004 Neonatal disease 22925008 Neonatal metabolic disorder 736652002 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Central nervous system complication 87536007 Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome 1186718008 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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