Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus 237611007
SNOMED CT code
| SNOMED code | 237611007 |
|---|---|
| name | Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus (disorder) |
| synonyms |
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| attributes - group5 | |
| Associated with | Genetic disease 782964007 |
| attributes - group3 | |
| Finding site | Endocrine structure 113331007 |
| attributes - group4 | |
| Finding site | Nervous system structure 25087005 |
| attributes - group2 | |
| Finding site | Retinal structure 5665001 |
| Associated morphology | Degenerative abnormality 107669003 |
| attributes - group1 | |
| Associated morphology | Atrophy 13331008 |
| Finding site | Skeletal muscle structure 127954009 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus 237611007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus 237611007 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus 237611007 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus 237611007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Diabetes mellitus 73211009 Secondary diabetes mellitus 8801005 Diabetes mellitus associated with genetic syndrome 5969009 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus 237611007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of coordination 298314008 Ataxia 20262006 Hereditary ataxia 763597000 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus 237611007 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Degenerative disorder of muscle 363058009 Muscle atrophy 88092000 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus 237611007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disorder of eye 62585004 Degeneration of retina 95695004 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus 237611007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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