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

722067005: Severe combined immunodeficiency with hypereosinophilia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3330457013 Severe combined immunodeficiency with hypereosinophilia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330458015 Severe combined immunodeficiency with hypereosinophilia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330459011 Omenn syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402817013 Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402818015 Omenn syndrome (OS) is an inflammatory condition characterised by erythroderma, desquamation, alopecia, chronic diarrhoea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Severe combined immunodeficiency with hypereosinophilia (disorder) Is a Severe combined immunodeficiency with low T- and B-cell numbers true Inferred relationship Some
Severe combined immunodeficiency with hypereosinophilia (disorder) Is a Hereditary eosinophilia true Inferred relationship Some
Severe combined immunodeficiency with hypereosinophilia (disorder) Is a Autosomal recessive severe combined immunodeficiency disease (disorder) true Inferred relationship Some
Severe combined immunodeficiency with hypereosinophilia (disorder) Has definitional manifestation Immune system finding false Inferred relationship Some
Severe combined immunodeficiency with hypereosinophilia (disorder) Has definitional manifestation Eosinophil count above reference range (finding) false Inferred relationship Some
Severe combined immunodeficiency with hypereosinophilia (disorder) Occurrence Congenital true Inferred relationship Some 3
Severe combined immunodeficiency with hypereosinophilia (disorder) Finding site Structure of immune system (body structure) true Inferred relationship Some 3
Severe combined immunodeficiency with hypereosinophilia (disorder) Has interpretation Above reference range true Inferred relationship Some 1
Severe combined immunodeficiency with hypereosinophilia (disorder) Interprets Eosinophil count true Inferred relationship Some 1
Severe combined immunodeficiency with hypereosinophilia (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 2
Severe combined immunodeficiency with hypereosinophilia (disorder) Is a Disorder of eosinophil (disorder) true Inferred relationship Some
Severe combined immunodeficiency with hypereosinophilia (disorder) Finding site Eosinophilic granulocytic cell true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

GB English

US English

Back to Start