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725104005: Cheirospondyloenchondromatosis (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3438596018 Cheirospondyloenchondromatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3438597010 Cheirospondyloenchondromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3438598017 Generalized enchondromatosis with platyspondyly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3438599013 Generalised enchondromatosis with platyspondyly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3438600011 An extremely rare type of enchondromatosis of very early onset (from neonatal period to infancy) with characteristics of symmetrical multiple enchondromas with metacarpal and phalangeal involvement resulting in short hands and feet, platyspondyly, mild to moderate short stature and intellectual disability. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3438596018 Cheirospondyloenchondromatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3438597010 Cheirospondyloenchondromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3438598017 Generalized enchondromatosis with platyspondyly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3438599013 Generalised enchondromatosis with platyspondyly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3438600011 An extremely rare type of enchondromatosis of very early onset (from neonatal period to infancy) with characteristics of symmetrical multiple enchondromas with metacarpal and phalangeal involvement resulting in short hands and feet, platyspondyly, mild to moderate short stature and intellectual disability. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3443941001000111 Cheiro-spondylo-enchondromatose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    884011000172118 cheiro-spondylo-enchondromatose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    976311000172114 enchondromatose généralisée avec platispondylie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    884011000172118 cheiro-spondylo-enchondromatose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    976311000172114 enchondromatose généralisée avec platispondylie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    3443941001000111 Cheiro-spondylo-enchondromatose de 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
    cheiro-spondylo-enchondromatose Is a Enchondromatosis false Inferred relationship Existential restriction modifier (core metadata concept)
    cheiro-spondylo-enchondromatose Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
    cheiro-spondylo-enchondromatose Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    cheiro-spondylo-enchondromatose Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    cheiro-spondylo-enchondromatose Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    cheiro-spondylo-enchondromatose Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    cheiro-spondylo-enchondromatose Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    cheiro-spondylo-enchondromatose Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    cheiro-spondylo-enchondromatose Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    cheiro-spondylo-enchondromatose Finding site Cartilage structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    cheiro-spondylo-enchondromatose Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
    cheiro-spondylo-enchondromatose Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    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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