Oculopharyngeal muscular dystrophy 77097004
SNOMED CT code
| SNOMED code | 77097004 |
|---|---|
| name | Oculopharyngeal muscular dystrophy |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Oculopharyngeal muscular dystrophy (disorder) |
| synonyms |
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| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Dystrophy 4720007 |
| Finding site | Structure of extraocular muscle 67833000 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Muscle structure of pharynx 60494004 |
| Associated morphology | Dystrophy 4720007 |
| attributes - group3 | |
| Clinical course | Progressive 255314001 |
| parents |
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| 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 Oculopharyngeal muscular dystrophy 77097004 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Finding of pharynx 116338005 Disorder of pharynx 75860007 Congenital anomaly of pharynx 11223009 Oculopharyngeal muscular dystrophy 77097004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic digestive system disorder 128284006 Oculopharyngeal muscular dystrophy 77097004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of ocular adnexa 128296004 Oculopharyngeal muscular dystrophy 77097004 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Congenital anomaly of visual system 127329003 Congenital anomaly of ocular adnexa 128327004 Oculopharyngeal muscular dystrophy 77097004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of respiratory system 17097001 Oculopharyngeal muscular dystrophy 77097004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Muscular dystrophy 73297009 Muscular dystrophy not predominantly limb girdle in distribution 240070002 Autosomal dominant muscular dystrophy not predominantly limb girdle 240075007 Oculopharyngeal muscular dystrophy 77097004 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Oculopharyngeal muscular dystrophy 77097004 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Oculopharyngeal muscular dystrophy 77097004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of neck 118939000 Congenital anomaly of neck 40052002 Oculopharyngeal muscular dystrophy 77097004 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Congenital anomaly of visual system 127329003 Congenital anomaly of orbit 54873004 Oculopharyngeal muscular dystrophy 77097004 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 Oculopharyngeal muscular dystrophy 77097004 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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