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773301007: Spondyloepimetaphyseal dysplasia Bieganski type (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3723040015 Spondyloepimetaphyseal dysplasia Bieganski type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3723041016 Spondyloepimetaphyseal dysplasia Bieganski type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3723042011 A rare primary bone dysplasia disorder with characteristics of infantile-onset, progressive, multiple skeletal deformities in association with slowly progressive central and peripheral neurodegeneration. Patients present short stature, coarse facies, psychomotor regression and cognitive impairment. Imaging shows abnormally shaped vertebral bodies, small, flat epiphyses, and widened metaphyses, as well as cerebral and cerebellar atrophy and progressive axonal-hypomyelinating neuropathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3723040015 Spondyloepimetaphyseal dysplasia Bieganski type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3723041016 Spondyloepimetaphyseal dysplasia Bieganski type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3723042011 A rare primary bone dysplasia disorder with characteristics of infantile-onset, progressive, multiple skeletal deformities in association with slowly progressive central and peripheral neurodegeneration. Patients present short stature, coarse facies, psychomotor regression and cognitive impairment. Imaging shows abnormally shaped vertebral bodies, small, flat epiphyses, and widened metaphyses, as well as cerebral and cerebellar atrophy and progressive axonal-hypomyelinating neuropathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    918561000172112 dysplasie spondylo-épimétaphysaire type Bieganski fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    918561000172112 dysplasie spondylo-épimétaphysaire type Bieganski fr 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
    dysplasie spondylo-épimétaphysaire type Bieganski Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    dysplasie spondylo-épimétaphysaire type Bieganski Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    dysplasie spondylo-épimétaphysaire type Bieganski Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    dysplasie spondylo-épimétaphysaire type Bieganski Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
    dysplasie spondylo-épimétaphysaire type Bieganski Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    dysplasie spondylo-épimétaphysaire type Bieganski Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
    dysplasie spondylo-épimétaphysaire type Bieganski Is a Spondyloepimetaphyseal disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    dysplasie spondylo-épimétaphysaire type Bieganski Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    REPLACED BY association reference set (foundation metadata concept)

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