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77016009: Amyoplasia congenita disruptive sequence (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    127855010 Amyoplasia congenita disruptive sequence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    127856011 Myodystrophia foetalis deformans en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    127857019 Classic arthrogryposis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    127859016 Myodystrophia fetalis deformans en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    127861013 Congenital arthromyodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    127862018 Myophagism congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    127863011 Amyoplasia congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    817800016 Amyoplasia congenita disruptive sequence (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1925441000052115 AMC (arthrogryposis multiplex congenita) sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    AMC (arthrogryposis multiplex congenita) Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings false Inferred relationship Some
    AMC (arthrogryposis multiplex congenita) Is a Arthrogryposis false Inferred relationship Some
    AMC (arthrogryposis multiplex congenita) Is a Congenital anomaly of skeletal muscle false Inferred relationship Some
    AMC (arthrogryposis multiplex congenita) Finding site Structure of musculoskeletal system (body structure) false Inferred relationship Some 1
    AMC (arthrogryposis multiplex congenita) Associated morphology kongenital kontraktur false Inferred relationship Some 1
    AMC (arthrogryposis multiplex congenita) Finding site Skeletal muscle structure false Inferred relationship Some 1
    AMC (arthrogryposis multiplex congenita) Finding site Joint structure false Inferred relationship Some 3
    AMC (arthrogryposis multiplex congenita) Finding site Brain structure false Inferred relationship Some 3
    AMC (arthrogryposis multiplex congenita) Occurrence Congenital false Inferred relationship Some
    AMC (arthrogryposis multiplex congenita) Is a Disorder of skeletal muscle false Inferred relationship Some
    AMC (arthrogryposis multiplex congenita) Associated morphology Contracture false Inferred relationship Some 2
    AMC (arthrogryposis multiplex congenita) Is a Muscle contracture false Inferred relationship Some
    AMC (arthrogryposis multiplex congenita) Associated morphology medfödd missbildning false Inferred relationship Some
    AMC (arthrogryposis multiplex congenita) Finding site Joint structure false Inferred relationship Some 4
    AMC (arthrogryposis multiplex congenita) Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings false Inferred relationship Some
    AMC (arthrogryposis multiplex congenita) Associated morphology kongenital anomali false Inferred relationship Some 4
    AMC (arthrogryposis multiplex congenita) Finding site Joint structure false Inferred relationship Some 1
    AMC (arthrogryposis multiplex congenita) Finding site Joint structure false Inferred relationship Some 4
    AMC (arthrogryposis multiplex congenita) Associated morphology Contracture false Inferred relationship Some 1
    AMC (arthrogryposis multiplex congenita) Finding site Joint structure false Inferred relationship Some 2
    AMC (arthrogryposis multiplex congenita) Associated morphology kongenital anomali false Inferred relationship Some 2
    AMC (arthrogryposis multiplex congenita) Finding site Joint structure false Inferred relationship Some 1
    AMC (arthrogryposis multiplex congenita) Occurrence Congenital false Inferred relationship Some 3
    AMC (arthrogryposis multiplex congenita) Associated morphology utvecklingsabnormitet false Inferred relationship Some 3
    AMC (arthrogryposis multiplex congenita) Finding site Joint structure false Inferred relationship Some 3
    AMC (arthrogryposis multiplex congenita) Occurrence Congenital false Inferred relationship Some 2
    AMC (arthrogryposis multiplex congenita) Associated morphology Contracture false Inferred relationship Some 2
    AMC (arthrogryposis multiplex congenita) Finding site Joint structure false Inferred relationship Some 2
    AMC (arthrogryposis multiplex congenita) Is a Congenital anomaly of joint false Inferred relationship Some
    AMC (arthrogryposis multiplex congenita) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    AMC (arthrogryposis multiplex congenita) Occurrence Congenital false Inferred relationship Some 1
    AMC (arthrogryposis multiplex congenita) Has interpretation Decreased false Inferred relationship Some 2
    AMC (arthrogryposis multiplex congenita) Interprets Range of joint movement false Inferred relationship Some 2
    AMC (arthrogryposis multiplex congenita) Finding site Structure of joint region false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder) Is a False AMC (arthrogryposis multiplex congenita) Inferred relationship Some
    X-linked distal arthrogryposis multiplex congenita (disorder) Is a False AMC (arthrogryposis multiplex congenita) Inferred relationship Some
    Van den Ende-Gupta syndrome (disorder) Is a False AMC (arthrogryposis multiplex congenita) Inferred relationship Some
    Adducted thumbs and arthrogryposis syndrome Christian type (disorder) Is a False AMC (arthrogryposis multiplex congenita) Inferred relationship Some
    Arthrogryposis multiplex congenita and whistling face syndrome (disorder) Is a False AMC (arthrogryposis multiplex congenita) Inferred relationship Some
    Intellectual disability, developmental delay, contracture syndrome (disorder) Is a False AMC (arthrogryposis multiplex congenita) Inferred relationship Some
    Arthrogryposis hyperkeratosis syndrome lethal form (disorder) Is a False AMC (arthrogryposis multiplex congenita) Inferred relationship Some
    Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) Is a False AMC (arthrogryposis multiplex congenita) Inferred relationship Some
    Hypomyelination neuropathy arthrogryposis syndrome (disorder) Is a False AMC (arthrogryposis multiplex congenita) Inferred relationship Some
    Congenital lethal myopathy Compton North type Is a False AMC (arthrogryposis multiplex congenita) Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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