FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

83092002: Shprintzen syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    137830014 Shprintzen syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    137831013 Velo-cardio-facial syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    824653015 Shprintzen syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1234786015 Velocardiofacial syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2164176017 VCF-Velocardiofacial syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2922770014 22q11 microdeletion with velocardiofacial syndrome phenotype en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    137830014 Shprintzen syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    137831013 Velo-cardio-facial syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    137831013 Velo-cardio-facial syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    137831013 Velo-cardio-facial syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    824653015 Shprintzen syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    824653015 Shprintzen syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1234785016 Shprintzen-Goldberg syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1234785016 Shprintzen-Goldberg syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1234786015 Velocardiofacial syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1234786015 Velocardiofacial syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2164176017 VCF-Velocardiofacial syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2922770014 22q11 microdeletion with velocardiofacial syndrome phenotype en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2922770014 22q11 microdeletion with velocardiofacial syndrome phenotype en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Shprintzen syndrome Is a Multisystem disorder S-T false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Is a Congenital heart disease (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Shprintzen syndrome Finding site Cardiovascular system subdivision false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Shprintzen syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Finding site Heart structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Shprintzen syndrome Finding site Musculoskeletal structure of limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Finding site Structure of cardiovascular system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Shprintzen syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Shprintzen syndrome Is a Structural disorder of heart false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Shprintzen syndrome Is a Viscus structure finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Is a Congenital anomaly of cardiovascular system false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Shprintzen syndrome Finding site Heart structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Shprintzen syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Shprintzen syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Is a Multiple system malformation syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
    Shprintzen syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Shprintzen syndrome Associated morphology anomalie du développement 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)

    Back to Start