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4541003: Congenital failure of fusion (morphologic abnormality)

    Status: retired, 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
    183285015 Congenital failure of fusion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    782647010 Congenital failure of fusion (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    29981000052114 medfödd utebliven fusion sv Synonym (core metadata concept) Active Entire term case insensitive (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
    medfödd utebliven fusion Is a kongenital anomali false Inferred relationship Some
    medfödd utebliven fusion Is a medfödd missbildning false Inferred relationship Some
    medfödd utebliven fusion Is a utvecklingsabnormitet false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 6
    Microcephalus cleft palate syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 5
    Cleft palate with short stature and vertebral anomaly syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 5
    Cleft palate with stapes fixation and oligodontia syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 6
    Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 4
    Abruzzo Erickson syndrome Associated morphology False medfödd utebliven fusion Inferred relationship Some 3
    Temtamy syndrome Associated morphology False medfödd utebliven fusion Inferred relationship Some 7
    Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 6
    Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 8
    Aural atresia with multiple congenital anomalies and intellectual disability syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 2
    Central complete cleft palate Associated morphology False medfödd utebliven fusion Inferred relationship Some 2
    Median cleft lip and alveolus Associated morphology False medfödd utebliven fusion Inferred relationship Some 2
    Coloboma of macula with brachydactyly type B syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 4
    Uranostaphyloschisis with cleft lip (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 1
    Cleft of soft palate and bilateral cleft lip (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 1
    Cleft of soft palate and cleft lip (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 1
    Biemond syndrome type 2 (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 1
    Mesomelic dysplasia with cleft palate and camptodactyly syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 1
    Bilateral microtia with deafness and cleft palate syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 5
    Hypertelorism with microtia and facial clefting syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 7
    Karsch Neugebauer syndrome Associated morphology False medfödd utebliven fusion Inferred relationship Some 5
    Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 5
    Hypertelorism with microtia and facial clefting syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 4
    Karsch Neugebauer syndrome Associated morphology False medfödd utebliven fusion Inferred relationship Some 8
    Goldberg Shprintzen megacolon syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 11
    Bamforth Lazarus syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 3
    Okamoto syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 6
    Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 5
    Hypoplasia and coloboma of alar cartilage with telecanthus syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 5
    Macular coloboma, cleft palate, hallux valgus syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 4
    Macular coloboma, cleft palate, hallux valgus syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 6
    syndrom med aurikulookulär anomali och läppspalt Associated morphology False medfödd utebliven fusion Inferred relationship Some 3
    Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder) Associated morphology False medfödd utebliven fusion Inferred relationship Some 7

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    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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