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77807009: Complete trisomy 10 syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    129130012 Complete trisomy 10 syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    818678012 Complete trisomy 10 syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    129130012 Complete trisomy 10 syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    129130012 Complete trisomy 10 syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    818678012 Complete trisomy 10 syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    818678012 Complete trisomy 10 syndrome (disorder) en Fully specified name 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
    Complete trisomy 10 syndrome Is a Anomaly of chromosome pair 10 (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Complete trisomy 10 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Complete trisomy 10 syndrome Finding site Sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
    Complete trisomy 10 syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Complete trisomy 10 syndrome Finding site Chromosome pair 10 false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Complete trisomy 10 syndrome Associated morphology Trisomy (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Complete trisomy 10 syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Complete trisomy 10 syndrome Finding site Chromosome pair 10 false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Complete trisomy 10 syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
    Complete trisomy 10 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Complete trisomy 10 syndrome Finding site Chromosome pair 10 false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Complete trisomy 10 syndrome Associated morphology Cellular AND/OR subcellular abnormality 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)

    POSSIBLY EQUIVALENT TO association reference set

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