FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

234637004: Deletion of X-chromosome and hypogammaglobulinemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
351575018 Deletion of X-chromosome and hypogammaglobulinemia en Synonym Active Only initial character case insensitive SNOMED CT core module
351576017 Deletion of X-chromosome and hypogammaglobulinaemia en Synonym Active Only initial character case insensitive SNOMED CT core module
622984017 Deletion of X-chromosome and hypogammaglobulinemia (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
Deletion of X-chromosome and hypogammaglobulinemia Is a Immunodeficiency associated with chromosomal abnormality true Inferred relationship Existential restriction modifier
Deletion of X-chromosome and hypogammaglobulinemia Finding site Structure of immune system true Inferred relationship Existential restriction modifier 1
Deletion of X-chromosome and hypogammaglobulinemia Is a Disorder of immune structure true Inferred relationship Existential restriction modifier
Deletion of X-chromosome and hypogammaglobulinemia Associated with Chromosomal disorder true Inferred relationship Existential restriction modifier 2
Deletion of X-chromosome and hypogammaglobulinemia Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Deletion of X-chromosome and hypogammaglobulinemia Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start