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698855007: 21-hydroxylase deficiency (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    2981453012 CYP21 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
    2981456016 21-hydroxylase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    2981467015 21-hydroxylase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    21-hydroxylase deficiency Is a Adrenogenital disorder false Inferred relationship Existential restriction modifier
    21-hydroxylase deficiency Is a Hereditary disorder of endocrine system false Inferred relationship Existential restriction modifier
    21-hydroxylase deficiency Is a Disorder of steroid metabolism false Inferred relationship Existential restriction modifier
    21-hydroxylase deficiency Is a Specific enzyme deficiency false Inferred relationship Existential restriction modifier
    21-hydroxylase deficiency Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
    21-hydroxylase deficiency Finding site Adrenal structure false Inferred relationship Existential restriction modifier

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Steroid 21-monooxygenase deficiency, simple virilizing type Due to False 21-hydroxylase deficiency Inferred relationship Existential restriction modifier
    Steroid 21-monooxygenase deficiency, salt wasting type Due to False 21-hydroxylase deficiency Inferred relationship Existential restriction modifier
    Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Due to False 21-hydroxylase deficiency Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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