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8632008: Schwartz syndrome (disorder)

    Status: retired, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    15240011 Schwartz syndrome en Synonym Active Case sensitive SNOMED CT core
    828560014 Schwartz syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Schwartz syndrome Is a Congenital anomaly of pituitary gland false Inferred relationship Some
    Schwartz syndrome Associated morphology Congenital malformation false Inferred relationship Some
    Schwartz syndrome Finding site Brain structure false Inferred relationship Some 1
    Schwartz syndrome Is a Congenital anomaly of endocrine gland false Inferred relationship Some
    Schwartz syndrome Is a Syndrome of inappropriate vasopressin secretion false Inferred relationship Some
    Schwartz syndrome Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings false Inferred relationship Some
    Schwartz syndrome Finding site Neurohypophysis structure false Inferred relationship Some
    Schwartz syndrome Occurrence Congenital false Inferred relationship Some 1
    Schwartz syndrome Associated morphology Developmental abnormality false Inferred relationship Some 1
    Schwartz syndrome Occurrence Congenital false Inferred relationship Some
    Schwartz syndrome Finding site Entire endocrine gonad false Inferred relationship Some
    Schwartz syndrome Finding site Pars nervosa of pituitary gland false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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