Autosomal dominant limb girdle muscular dystrophy type 1B 718178006

SNOMED CT code

SNOMED code

718178006

name

Autosomal dominant limb girdle muscular dystrophy type 1B

status

removed

date introduced

2016-07-31

fully specified name(s)

Autosomal dominant limb girdle muscular dystrophy type 1B (disorder)

synonyms

Autosomal dominant limb girdle muscular dystrophy type 1B

parents

Autosomal dominant muscular dystrophy with limb girdle distribution 240067001

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
Autosomal dominant muscular dystrophy with limb girdle distribution 240067001
Autosomal dominant limb girdle muscular dystrophy type 1B 718178006 removed: 2021-01-31

ancestors

sorted most to least specific

Autosomal dominant muscular dystrophy with limb girdle distribution 240067001
Autosomal dominant hereditary disorder 11164009
Muscular dystrophy with predominantly proximal limb girdle distribution 240046001
Autosomal hereditary disorder 1899006
Hereditary progressive muscular dystrophy 193225000
Developmental hereditary disorder 363070008
Hereditary disorder of musculoskeletal system 363212003
Muscular dystrophy 73297009
Hereditary disorder by system 363137000
Chronic disease of musculoskeletal system 128237006
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 musculoskeletal system 928000
Disorder of muscle 129565002
Degenerative disorder 362975008
Disorder of soft tissue 19660004
Genetic disease 782964007
Musculoskeletal finding 106028002
Disorder of body system 362965005
Muscle finding 106030000
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

Autosomal dominant muscular dystrophy with limb girdle distribution 240067001

Autosomal dominant limb girdle muscular dystrophy type 1B 718178006

SNOMED CT code