Adult-onset distal myopathy due to valosin containing protein mutation 770792007
SNOMED CT code
SNOMED code | 770792007 |
---|---|
name | Adult-onset distal myopathy due to valosin containing protein mutation |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Adult-onset distal myopathy due to valosin containing protein mutation (disorder) |
synonyms |
|
attributes - group2 | |
Associated morphology | Dystrophy 4720007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Skeletal muscle structure 127954009 |
attributes - group3 | |
Clinical course | Progressive 255314001 |
attributes - group1 | |
Occurrence | Adulthood 41847000 |
Finding site | Skeletal muscle structure 127954009 |
Associated morphology | Dystrophy 4720007 |
parents | |
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 Adult-onset distal myopathy due to valosin containing protein mutation 770792007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Distal muscular dystrophy 58795000 Adult-onset distal myopathy due to valosin containing protein mutation 770792007 |
ancestors | sorted most to least specific
|
cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.