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718572004: Bethlem myopathy (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3312733011 Bethlem myopathy (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3312803013 Bethlem myopathy en Synonym Active Case sensitive SNOMED CT core
3312804019 Benign autosomal dominant myopathy en Synonym Active Case insensitive SNOMED CT core
3312805018 A benign autosomal dominant form of slowly progressive muscular dystrophy. To date, fewer than 100 cases have been reported in the literature, thus illustrating its rarity. The clinical features do not differ markedly from those of other mild forms of progressive muscular dystrophy with the exception of finger contractures that are sometimes suggestive of the diagnosis. Creatine kinase levels and histological findings are not conclusive. Mutations in one of the three subunits of collagen VI are responsible for the disease. Molecular studies are however hampered by the size and expression pattern of the genes. Treatment remains purely supportive. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Bethlem myopathy Finding site Skeletal muscle structure true Inferred relationship Some 1
Bethlem myopathy Associated morphology Morphologically abnormal structure false Inferred relationship Some 2
Bethlem myopathy Pathological process Pathological developmental process true Inferred relationship Some 1
Bethlem myopathy Pathological process Pathological developmental process false Inferred relationship Some 2
Bethlem myopathy Associated morphology Dystrophy true Inferred relationship Some 1
Bethlem myopathy Occurrence Congenital true Inferred relationship Some 1
Bethlem myopathy Clinical course Progressive true Inferred relationship Some 2
Bethlem myopathy Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Bethlem myopathy Is a Congenital hereditary muscular dystrophy true Inferred relationship Some
Bethlem myopathy Is a Hereditary progressive muscular dystrophy false Inferred relationship Some
Bethlem myopathy Associated morphology Developmental abnormality false Inferred relationship Some 2
Bethlem myopathy Occurrence Congenital false Inferred relationship Some 2
Bethlem myopathy Finding site Skeletal muscle structure false Inferred relationship Some 2
Bethlem myopathy Associated morphology Dystrophy false Inferred relationship Some 3
Bethlem myopathy Finding site Skeletal muscle structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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