Finnish upper limb onset distal myopathy 763718009

SNOMED CT code

SNOMED code

763718009

name

Finnish upper limb onset distal myopathy

status

active

date introduced

2018-07-31

fully specified name(s)

Finnish upper limb onset distal myopathy (disorder)

synonyms

Finnish upper limb onset distal myopathy
Distal myopathy type 3

attributes - group2

Pathological process

Pathological developmental process 308490002

Finding site

Skeletal muscle structure 127954009

Associated morphology

Dystrophy 4720007

attributes - group3

Clinical course

Progressive 255314001

attributes - group1

Associated morphology

Dystrophy 4720007

Finding site

Skeletal muscle structure 127954009

Occurrence

Adulthood 41847000

parents

Autosomal dominant hereditary disorder 11164009
Distal muscular dystrophy 58795000

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Finnish upper limb onset distal myopathy 763718009

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Distal muscular dystrophy 58795000
Finnish upper limb onset distal myopathy 763718009

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Distal muscular dystrophy 58795000
Autosomal hereditary disorder 1899006
Hereditary progressive muscular dystrophy 193225000
Muscular dystrophy not predominantly limb girdle in distribution 240070002
Developmental hereditary disorder 363070008
Muscular dystrophy 73297009
Hereditary disorder of musculoskeletal system 363212003
Chronic disease of musculoskeletal system 128237006
Hereditary disorder by system 363137000
Developmental disorder 5294002
Degenerative disorder of muscle 363058009
Degenerative disorder of musculoskeletal system 363059001
Disorder of skeletal muscle 75047002
Hereditary disease 32895009
Chronic disease 27624003
Disorder of muscle 129565002
Degenerative disorder 362975008
Disorder of musculoskeletal system 928000
Disorder of soft tissue 19660004
Genetic disease 782964007
Muscle finding 106030000
Musculoskeletal finding 106028002
Disorder of body system 362965005
General finding of soft tissue 248402002
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Genetic disease 782964007

Hereditary disease 32895009

Autosomal hereditary disorder 1899006

Autosomal dominant hereditary disorder 11164009

Finnish upper limb onset distal myopathy 763718009

SNOMED CT code