FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

766879006: Combined immunodeficiency due to OX40 deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3662993011 Combined immunodeficiency due to OX40 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3662994017 Combined immunodeficiency due to OX40 deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3662996015 Combined immunodeficiency with childhood-onset Kaposi sarcoma en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Combined immunodeficiency due to OX40 deficiency Is a Hereditary disorder of immune system true Inferred relationship Existential restriction modifier
Combined immunodeficiency due to OX40 deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Combined immunodeficiency due to OX40 deficiency Is a Disorder of immune structure true Inferred relationship Existential restriction modifier
Combined immunodeficiency due to OX40 deficiency Is a Combined immunodeficiency disease true Inferred relationship Existential restriction modifier
Combined immunodeficiency due to OX40 deficiency Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier
Combined immunodeficiency due to OX40 deficiency Finding site Structure of immune system true Inferred relationship Existential restriction modifier 1
Combined immunodeficiency due to OX40 deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Combined immunodeficiency due to OX40 deficiency Due to Chromosomal disorder true Inferred relationship Existential restriction modifier 2
Combined immunodeficiency due to OX40 deficiency Is a Immunodeficiency associated with chromosomal abnormality true Inferred relationship Existential restriction modifier
Combined immunodeficiency due to OX40 deficiency Is a Congenital immunodeficiency disease true Inferred relationship Existential restriction modifier
Combined immunodeficiency due to OX40 deficiency 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