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267460002: Congenital hypogammaglobulinemia (finding)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Dec 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
398903019 Congenital hypogammaglobulinaemia en Synonym Active Entire term case insensitive SNOMED CT core module
398904013 Congenital hypogammaglobulinemia en Synonym Active Entire term case insensitive SNOMED CT core module
660080016 Congenital hypogammaglobulinemia (finding) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypogammaglobulinemia Is a Agammaglobulinemia false Inferred relationship Existential restriction modifier
Congenital hypogammaglobulinemia Finding site Structure of immune system false Inferred relationship Existential restriction modifier 1
Congenital hypogammaglobulinemia Interprets Biochemistry test interpretation false Inferred relationship Existential restriction modifier
Congenital hypogammaglobulinemia Interprets Laboratory test false Inferred relationship Existential restriction modifier
Congenital hypogammaglobulinemia Finding method Procedure false Inferred relationship Existential restriction modifier
Congenital hypogammaglobulinemia Interprets Globulin measurement false Inferred relationship Existential restriction modifier 2
Congenital hypogammaglobulinemia Interprets Globulin measurement true Inferred relationship Existential restriction modifier 1
Congenital hypogammaglobulinemia Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Congenital hypogammaglobulinemia Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital hypogammaglobulinemia Is a Hypogammaglobulinemia true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Osteopetrosis hypogammaglobulinemia syndrome Is a True Congenital hypogammaglobulinemia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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