Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007
SNOMED CT code
| SNOMED code | 718214007 |
|---|---|
| name | Mitochondrial neurogastrointestinal encephalomyopathy syndrome |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder) |
| synonyms | Mitochondrial neurogastrointestinal encephalomyopathy syndrome |
| attributes - group5 | |
| Clinical course | Progressive 255314001 |
| attributes - group2 | |
| Finding site | Structure of extraocular muscle 67833000 |
| attributes - group6 | |
| Interprets | Movement 255324009 |
| attributes - group4 | |
| Interprets | Movement observable 363847004 |
| Has interpretation | Absent 2667000 |
| attributes - group3 | |
| Finding site | Cerebral white matter structure 68523003 |
| attributes - group1 | |
| Finding site | Gastrointestinal tract structure 122865005 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Digestive system finding 386617003 Gastrointestinal tract finding 386618008 Disorder of gastrointestinal tract 119292006 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic digestive system disorder 128284006 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic metabolic disorder 128289001 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Leukoencephalopathy 22811006 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 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 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Mitochondrial encephalomyopathy 447292006 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of musculoskeletal system 128237006 Progressive external ophthalmoplegia 46252003 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Orbit finding 246912006 Disorder of orbit proper 371436007 Disorder of extraocular muscle 128603005 Myopathy of extraocular muscles 57130002 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic nervous system disorder 128283000 Chronic brain syndrome 78689005 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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