Oculopharyngodistal myopathy 763829004
SNOMED CT code
| SNOMED code | 763829004 |
|---|---|
| name | Oculopharyngodistal myopathy |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Oculopharyngodistal myopathy (disorder) |
| synonyms |
|
| attributes - group4 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dystrophy 4720007 |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group2 | |
| Finding site | Upper eyelid structure 38934000 |
| Associated morphology | Prolapse 29696001 |
| attributes - group1 | |
| Clinical course | Progressive 255314001 |
| attributes - group3 | |
| Finding site | Muscle structure of pharynx 60494004 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Musculoskeletal disorder of the neck 111235007 Oculopharyngodistal myopathy 763829004 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Eyelid finding 246812007 Disorder of eyelid 60113004 Ptosis of eyelid 11934000 Oculopharyngodistal myopathy 763829004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic digestive system disorder 128284006 Oculopharyngodistal myopathy 763829004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of ocular adnexa 128296004 Oculopharyngodistal myopathy 763829004 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Finding of neck region 298378000 Pharyngeal paresis 129567005 Oculopharyngodistal myopathy 763829004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of respiratory system 17097001 Oculopharyngodistal myopathy 763829004 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Oculopharyngodistal myopathy 763829004 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Oculopharyngodistal myopathy 763829004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Distal muscular dystrophy 58795000 Oculopharyngodistal myopathy 763829004 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Finding of pharynx 116338005 Disorder of pharynx 75860007 Oculopharyngodistal myopathy 763829004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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