44940001: Adenosine deaminase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Autosomal recessive SCID (severe combined immunodeficiency disease)\Adenosine deaminase deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autosomal recessive SCID (severe combined immunodeficiency disease)\Adenosine deaminase deficiency
• \Disorder of immune function\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Autosomal recessive SCID (severe combined immunodeficiency disease)\Adenosine deaminase deficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Severe combined immunodeficiency disease\Autosomal recessive SCID (severe combined immunodeficiency disease)\Adenosine deaminase deficiency
• \Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Autosomal recessive SCID (severe combined immunodeficiency disease)\Adenosine deaminase deficiency
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Autosomal recessive SCID (severe combined immunodeficiency disease)\Adenosine deaminase deficiency
• \Metabolic disease\Purine and pyrimidine metabolism disorder\Disorder of purine metabolism\Adenosine deaminase deficiency
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Adenosine deaminase deficiency
• \Congenital disease\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Autosomal recessive SCID (severe combined immunodeficiency disease)\Adenosine deaminase deficiency

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1230164018	ADA - Adenosine aminohydrolase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
2478708016	Deficiency of adenosine deaminase	en	Synonym	Active	Case insensitive	SNOMED CT core
74969018	Adenosine deaminase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
74970017	ADA deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
74971018	Adenosine aminohydrolase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
782124013	Adenosine deaminase deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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