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699313003: heterozygote otospondylomega-epifysaire dysplasie (aandoening)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2983750018 Weissenbacher-Zweymuller syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2983759017 Heterozygous OSMED (otospondylomegaepiphyseal dysplasia) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2983762019 Heterozygous otospondylomegaepiphyseal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2983764018 Weissenbacher-Zweymuller syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2983766016 Pierre Robin syndrome with fetal chondrodysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    8136461000146116 heterozygote otospondylomega-epifysaire dysplasie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    8136471000146110 Weissenbacher-Zweymuller-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    8136481000146112 heterozygote otospondylomega-epifysaire dysplasie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    9477981000146119 heterozygote OSMED nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    9477991000146117 syndroom van Pierre Robin sequentie en foetale chondrodysplasie 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
    heterozygote otospondylomega-epifysaire dysplasie Is a Congenital anomaly of skeletal bone false Inferred relationship Some
    heterozygote otospondylomega-epifysaire dysplasie Is a Disorder of auditory system false Inferred relationship Some
    heterozygote otospondylomega-epifysaire dysplasie Is a Congenital anomaly of face (disorder) false Inferred relationship Some
    heterozygote otospondylomega-epifysaire dysplasie Occurrence Congenital false Inferred relationship Some
    heterozygote otospondylomega-epifysaire dysplasie Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 4
    heterozygote otospondylomega-epifysaire dysplasie Finding site Face structure false Inferred relationship Some 4
    heterozygote otospondylomega-epifysaire dysplasie Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 5
    heterozygote otospondylomega-epifysaire dysplasie Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 6
    heterozygote otospondylomega-epifysaire dysplasie Finding site Structure of auditory system (body structure) false Inferred relationship Some 5
    heterozygote otospondylomega-epifysaire dysplasie Finding site Bone structure false Inferred relationship Some 6
    heterozygote otospondylomega-epifysaire dysplasie Is a Disorder of face (disorder) false Inferred relationship Some
    heterozygote otospondylomega-epifysaire dysplasie Occurrence Congenital false Inferred relationship Some 1
    heterozygote otospondylomega-epifysaire dysplasie Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 1
    heterozygote otospondylomega-epifysaire dysplasie Finding site Bone structure false Inferred relationship Some 1
    heterozygote otospondylomega-epifysaire dysplasie Occurrence Congenital false Inferred relationship Some 3
    heterozygote otospondylomega-epifysaire dysplasie Finding site Bone structure false Inferred relationship Some 3
    heterozygote otospondylomega-epifysaire dysplasie Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 2
    heterozygote otospondylomega-epifysaire dysplasie Pathological process (attribute) Pathological developmental process false Inferred relationship Some 3
    heterozygote otospondylomega-epifysaire dysplasie Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    heterozygote otospondylomega-epifysaire dysplasie Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 1
    heterozygote otospondylomega-epifysaire dysplasie Occurrence Congenital false Inferred relationship Some 2
    heterozygote otospondylomega-epifysaire dysplasie Finding site Face structure false Inferred relationship Some 1
    heterozygote otospondylomega-epifysaire dysplasie Finding site Structure of auditory system (body structure) false Inferred relationship Some 2
    heterozygote otospondylomega-epifysaire dysplasie Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
    heterozygote otospondylomega-epifysaire dysplasie Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 3
    heterozygote otospondylomega-epifysaire dysplasie Is a Congenital anomaly of face (disorder) false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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