124147007: Deficiency of xanthine oxidase (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Kidney finding\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Kidney finding\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase

\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Disease\Metabolic disease\Disorder of purine and pyrimidine metabolism\Deficiency of xanthine oxidase
\Disease\Metabolic disease\Metabolic renal disease\Deficiency of xanthine oxidase
\Disease\Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of xanthine oxidase

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

203590019 Deficiency of hypoxanthine oxidase en Synonym Active Entire term case insensitive SNOMED CT core module
203591015 Deficiency of xanthine oxidase en Synonym Active Entire term case insensitive SNOMED CT core module
473026015 Xanthine oxidase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
473027012 Hereditary xanthinuria type 1 en Synonym Inactive Entire term case insensitive SNOMED CT core module
727637011 Deficiency of xanthine oxidase (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Deficiency of xanthine oxidase	Is a	Specific enzyme deficiency	true	Inferred relationship	Existential restriction modifier
Deficiency of xanthine oxidase	Is a	Metabolic renal disease	true	Inferred relationship	Existential restriction modifier
Deficiency of xanthine oxidase	Is a	Hereditary disorder of the urinary system	false	Inferred relationship	Existential restriction modifier
Deficiency of xanthine oxidase	Is a	Disorder of purine and pyrimidine metabolism	true	Inferred relationship	Existential restriction modifier
Deficiency of xanthine oxidase	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Deficiency of xanthine oxidase	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Deficiency of xanthine oxidase	Finding site	Kidney structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary xanthinuria type 1	Due to	True	Deficiency of xanthine oxidase	Inferred relationship	Existential restriction modifier	1

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
203590019	Deficiency of hypoxanthine oxidase	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
203591015	Deficiency of xanthine oxidase	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
473026015	Xanthine oxidase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
473027012	Hereditary xanthinuria type 1	en	Synonym	Inactive	Entire term case insensitive	SNOMED CT core module
727637011	Deficiency of xanthine oxidase (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module