Severe early-onset axonal neuropathy due to mitofusin 2 deficiency 766977007
SNOMED CT code
| SNOMED code | 766977007 |
|---|---|
| name | Severe early-onset axonal neuropathy due to mitofusin 2 deficiency |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Severe early-onset axonal neuropathy due to mitofusin 2 deficiency (disorder) |
| synonyms |
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| 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 Severe early-onset axonal neuropathy due to mitofusin 2 deficiency 766977007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Severe early-onset axonal neuropathy due to mitofusin 2 deficiency 766977007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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