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718572004: Bethlem myopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case sensitive (core metadata concept) SNOMED CT core
3312803013 Bethlem myopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312804019 Benign autosomal dominant myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401766017 A form of congenital muscular dystrophy characterized by a congenital to childhood onset of progressive proximal muscle weakness, joint contractures, and potential respiratory insufficiency in adulthood. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401767014 A form of congenital muscular dystrophy characterised by a congenital to childhood onset of progressive proximal muscle weakness, joint contractures, and potential respiratory insufficiency in adulthood. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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