FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

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

    Back to Start