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764858009: Isolated agammaglobulinemia (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

3655363015 Isolated agammaglobulinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3655364014 Isolated agammaglobulinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3655365010 Isolated agammaglobulinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5404396014 Isolated agammaglobulinemia (IA) is the non-syndromic form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by deficient gamma globulins and associated predisposition to frequent and recurrent infections from infancy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5404397017 Isolated agammaglobulinaemia (IA) is the non-syndromic form of agammaglobulinaemia, a primary immunodeficiency disease, and is characterised by deficient gamma globulins and associated predisposition to frequent and recurrent infections from infancy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Isolated agammaglobulinaemia	Is a	Congenital agammaglobulinemia	true	Inferred relationship	Some
Isolated agammaglobulinaemia	Is a	Hereditary disorder of immune system	false	Inferred relationship	Some
Isolated agammaglobulinaemia	Is a	Disorder of immune structure (disorder)	false	Inferred relationship	Some
Isolated agammaglobulinaemia	Occurrence	Congenital	true	Inferred relationship	Some	1
Isolated agammaglobulinaemia	Finding site	Structure of immune system (body structure)	false	Inferred relationship	Some	1
Isolated agammaglobulinaemia	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	2
Isolated agammaglobulinaemia	Is a	Primary immune deficiency disorder	true	Inferred relationship	Some
Isolated agammaglobulinaemia	Pathological process (attribute)	Abnormal immune process (qualifier value)	false	Inferred relationship	Some	1
Isolated agammaglobulinaemia	Is a	Hereditary disease	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
X-linked agammaglobulinemia	Is a	True	Isolated agammaglobulinaemia	Inferred relationship	Some
Autosomal recessive agammaglobulinemia	Is a	True	Isolated agammaglobulinaemia	Inferred relationship	Some
Autosomal dominant agammaglobulinaemia due to E47 transcription factor deficiency	Is a	True	Isolated agammaglobulinaemia	Inferred relationship	Some

Reference Sets

Id	Description	Lang	Type	Status	Case?	Module
3655363015	Isolated agammaglobulinaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3655364014	Isolated agammaglobulinemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3655365010	Isolated agammaglobulinemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5404396014	Isolated agammaglobulinemia (IA) is the non-syndromic form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by deficient gamma globulins and associated predisposition to frequent and recurrent infections from infancy.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5404397017	Isolated agammaglobulinaemia (IA) is the non-syndromic form of agammaglobulinaemia, a primary immunodeficiency disease, and is characterised by deficient gamma globulins and associated predisposition to frequent and recurrent infections from infancy.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core