Benign Samaritan congenital myopathy 770787005

SNOMED CT code

SNOMED code

770787005

name

Benign Samaritan congenital myopathy

status

active

date introduced

2019-01-31

fully specified name(s)

Benign Samaritan congenital myopathy (disorder)

synonyms

Benign Samaritan congenital myopathy

attributes - group1

Associated morphology

Morphologically abnormal structure 49755003

Pathological process

Pathological developmental process 308490002

Finding site

Skeletal muscle structure 127954009

Occurrence

Congenital 255399007

parents

Benign congenital myopathy 193222002
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Benign congenital myopathy 193222002
Benign Samaritan congenital myopathy 770787005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Benign Samaritan congenital myopathy 770787005

ancestors

sorted most to least specific

Benign congenital myopathy 193222002
Autosomal recessive hereditary disorder 85995004
Developmental hereditary disorder 363070008
Autosomal hereditary disorder 1899006
Hereditary disorder of musculoskeletal system 363212003
Congenital anomaly of skeletal muscle 89886004
Hereditary disorder by system 363137000
Disorder of skeletal muscle 75047002
Congenital anomaly of muscle AND/OR tendon 79191007
Hereditary disease 32895009
Disorder of muscle 129565002
Congenital anomaly of musculoskeletal system 73573004
Disorder of soft tissue 19660004
Genetic disease 782964007
Muscle finding 106030000
Disorder of musculoskeletal system 928000
Congenital malformation 276654001
General finding of soft tissue 248402002
Developmental disorder 5294002
Musculoskeletal finding 106028002
Disorder of body system 362965005
Congenital disease 66091009
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Developmental disorder 5294002

Developmental hereditary disorder 363070008

Benign congenital myopathy 193222002

Benign Samaritan congenital myopathy 770787005

SNOMED CT code