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76085008: Leydig cell hyperplasia (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    126370010 Leydig cell hyperplasia en Synonym Active Case sensitive SNOMED CT core
    126371014 Interstitial cell hyperplasia en Synonym Active Case insensitive SNOMED CT core
    816766012 Leydig cell hyperplasia (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
    Leydig cell hyperplasia Is a Disorder of connective tissue false Inferred relationship Some
    Leydig cell hyperplasia Is a Testicular dysfunction false Inferred relationship Some
    Leydig cell hyperplasia Finding site Entire endocrine testis false Inferred relationship Some
    Leydig cell hyperplasia Is a Soft tissue lesion of pelvic region false Inferred relationship Some
    Leydig cell hyperplasia Is a Lesion of testis false Inferred relationship Some
    Leydig cell hyperplasia Is a Disorder of soft tissue false Inferred relationship Some
    Leydig cell hyperplasia Is a Disorder of endocrine system false Inferred relationship Some
    Leydig cell hyperplasia Is a Disorder of testis false Inferred relationship Some
    Leydig cell hyperplasia Finding site Structure of interstitial cell of Leydig false Inferred relationship Some 1
    Leydig cell hyperplasia Associated morphology Hyperplasia false Inferred relationship Some
    Leydig cell hyperplasia Finding site Testicular endocrine structure false Inferred relationship Some
    Leydig cell hyperplasia Finding site Structure of interstitial cell of Leydig false Inferred relationship Some 1
    Leydig cell hyperplasia Associated morphology Hyperplasia false Inferred relationship Some 1
    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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