65520001: Primary hyperoxaluria, type I (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Kidney finding\Kidney disease\...

\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I

\Metabolic renal disease\Primary hyperoxaluria\Primary hyperoxaluria, type I

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Metabolic renal disease\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Hereditary disorder of the urinary system\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Kidney finding\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Kidney finding\Kidney disease\Metabolic renal disease\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Metabolic renal disease\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\Metabolic renal disease\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Disorder of the genitourinary system\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Metabolic renal disease\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Primary hyperoxaluria, type I
\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the urinary system\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the urinary system\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Metabolic renal disease\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\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\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Primary hyperoxaluria, type I
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Metabolic disease\Metabolic renal disease\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Metabolic disease\Enzymopathy\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Primary hyperoxaluria\Primary hyperoxaluria, type I
\Disease\Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Primary hyperoxaluria, type I
\Disease\Congenital disease\Inborn error of metabolism\Primary hyperoxaluria\Primary hyperoxaluria, type I

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

Descriptions:

Id Description Lang Type Status Case? Module

108861015 Primary hyperoxaluria, type I en Synonym Active Initial character case insensitive SNOMED CT core

108862010 Glycolic aciduria en Synonym Active Case insensitive SNOMED CT core

108863017 Alanine-glyoxylate aminotransferase deficiency en Synonym Active Case insensitive SNOMED CT core

1232687016 2-Oxoglutarate glyoxylate carboligase deficiency en Synonym Active Initial character case insensitive SNOMED CT core

1232688014 Oxalosis type I en Synonym Active Initial character case insensitive SNOMED CT core

1232689018 Primary hyperoxaluria type I en Synonym Active Initial character case insensitive SNOMED CT core

1232690010 Alanine-glycoxylate aminotransferase deficiency en Synonym Active Case insensitive SNOMED CT core

805032013 Primary hyperoxaluria, type I (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Primary hyperoxaluria, type I	Is a	Primary hyperoxaluria	true	Inferred relationship	Some
Primary hyperoxaluria, type I	Is a	Loss of single peroxisomal function	true	Inferred relationship	Some
Primary hyperoxaluria, type I	Occurrence	Congenital	true	Inferred relationship	Some	1
Primary hyperoxaluria, type I	Finding site	Kidney structure	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Oxaluria NEC	Is a	False	Primary hyperoxaluria, type I	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set