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205814003: Holt-Oram syndrome (disorder)

    Status: retired, Primitive. Date: 31-Jul 2002. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2741387016 Holt-Oram syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
    315608015 Holt-Oram syndrome en Synonym Active Case sensitive SNOMED CT core
    591234013 Holt-Oram syndrome [dup] (disorder) en Fully specified name Inactive Initial character case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Holt-Oram syndrome Finding site Interatrial septum structure false Inferred relationship Some 1
    Holt-Oram syndrome Is a Multisystem disorder G-H false Inferred relationship Some
    Holt-Oram syndrome Is a Ostium secundum type atrial septal defect false Inferred relationship Some
    Holt-Oram syndrome Is a Congenital anomaly of upper limb false Inferred relationship Some
    Holt-Oram syndrome Associated morphology Developmental abnormality false Inferred relationship Some
    Holt-Oram syndrome Associated morphology Congenital absence false Inferred relationship Some 1
    Holt-Oram syndrome Finding site Musculoskeletal structure of upper limb false Inferred relationship Some
    Holt-Oram syndrome Occurrence Congenital false Inferred relationship Some
    Holt-Oram syndrome Associated morphology Mechanical abnormality false Inferred relationship Some
    Holt-Oram syndrome Associated morphology Congenital incomplete closure false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Australian dialect reference set

    Concept inactivation indicator reference set

    SAME AS association reference set

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