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726107008: Distal myopathy Welander type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5403535016 A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403536015 A rare distal myopathy characterised by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3448212018 Distal myopathy Welander type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3448213011 Distal myopathy Welander type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3448214017 Distal myopathy Swedish type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
932181000172116 myopathie distale type Welander fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
954211000172114 WDM - distal myopathy, Welander type fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3413091001000113 Myopathie, distale, Typ Welander de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Is a Distal muscular dystrophy true Inferred relationship Some
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Is a Autosomal dominant muscular dystrophy not predominantly limb girdle false Inferred relationship Some
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Occurrence Congenital false Inferred relationship Some 2
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Finding site Skeletal muscle structure true Inferred relationship Some 2
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Occurrence Congenital false Inferred relationship Some 3
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Finding site Skeletal muscle structure false Inferred relationship Some 3
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Associated morphology Dystrophy true Inferred relationship Some 2
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Associated morphology anomalie du développement false Inferred relationship Some 3
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Finding site Skeletal muscle structure true Inferred relationship Some 1
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Associated morphology Dystrophy true Inferred relationship Some 1
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Occurrence Adulthood true Inferred relationship Some 1
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors. Clinical course Progressive true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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