Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome 1187643003
SNOMED CT code
| SNOMED code | 1187643003 |
|---|---|
| name | Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome |
| status | active |
| date introduced | 2022-01-31 |
| fully specified name(s) | Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder) |
| synonyms |
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| attributes - group4 | |
| Finding site | Peripheral nervous system structure 3058005 |
| attributes - group3 | |
| Occurrence | Infancy 3658006 |
| Finding site | Structure of parenchyma of liver 127879008 |
| attributes - group1 | |
| Finding site | Cerebellar structure 113305005 |
| Associated morphology | Degenerative abnormality 107669003 |
| attributes - group2 | |
| Finding site | Spinal cord structure 2748008 |
| Associated morphology | Degenerative abnormality 107669003 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of coordination 298314008 Ataxia 20262006 Hereditary ataxia 763597000 Spinocerebellar ataxia 129609000 Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome 1187643003 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Liver finding 249565005 Disease of liver 235856003 Hepatic failure 59927004 Acute hepatic failure 197270009 Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome 1187643003 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome 1187643003 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 Hereditary peripheral neuropathy 65017003 Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome 1187643003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome 1187643003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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