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77016009: amyoplasia congenita (aandoening)

    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
    12009891000146113 amyoplasia congenita (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    12009901000146114 amyoplasia congenita nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    12204481000146115 congenitale amyoplasie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

    0 descendants.

    Expanded Value Set

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

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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