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205719003: 46, XX true hermaphrodite (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2022. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    315485011 46, XX true hermaphrodite en Synonym Active Only initial character case insensitive SNOMED CT core module
    591125012 46, XX true hermaphrodite (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    46, XX true hermaphrodite Is a Congenital disorder due to abnormality of chromosome number OR structure false Inferred relationship Existential restriction modifier
    46, XX true hermaphrodite Is a Hermaphroditism false Inferred relationship Existential restriction modifier
    46, XX true hermaphrodite Is a Congenital anomaly of endocrine gland false Inferred relationship Existential restriction modifier
    46, XX true hermaphrodite Occurrence Congenital false Inferred relationship Existential restriction modifier
    46, XX true hermaphrodite Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
    46, XX true hermaphrodite Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
    46, XX true hermaphrodite Finding site Gonadal endocrine structure false Inferred relationship Existential restriction modifier 2
    46, XX true hermaphrodite Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
    46, XX true hermaphrodite Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    46, XX true hermaphrodite Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
    46, XX true hermaphrodite Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
    46, XX true hermaphrodite Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    46, XX true hermaphrodite Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
    46, XX true hermaphrodite Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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