Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect 1187619001
SNOMED CT code
| SNOMED code | 1187619001 |
|---|---|
| name | Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect |
| status | active |
| date introduced | 2022-01-31 |
| fully specified name(s) | Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect (disorder) |
| synonyms | Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect |
| attributes - group2 | |
| Due to | Disorder of copper metabolism 79886009 |
| attributes - group1 | |
| Finding site | Peripheral nervous system structure 3058005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Hereditary peripheral neuropathy 65017003 Hereditary motor and sensory neuropathy 398100001 Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect 1187619001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of mineral metabolism 45744005 Disorder of copper metabolism 79886009 Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect 1187619001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect 1187619001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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