17901006: Primary hyperoxaluria (disorder)

SNOMED CT Concept\Clinical finding\...

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

\Hereditary nephropathy\Primary hyperoxaluria

\Metabolic renal disease\Primary hyperoxaluria

\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\Hereditary nephropathy\Primary hyperoxaluria
\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\Primary hyperoxaluria
\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
\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
\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
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Kidney finding\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria
\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
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria
\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\Primary hyperoxaluria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\Metabolic renal disease\Primary hyperoxaluria
\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
\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
\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
\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
\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
\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
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria
\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\Primary hyperoxaluria
\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
\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
\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

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Primary hyperoxaluria
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the urinary system\Hereditary nephropathy\Primary hyperoxaluria
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Primary hyperoxaluria
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the urinary system\Hereditary nephropathy\Primary hyperoxaluria
\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
\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
\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
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Hereditary nephropathy\Primary hyperoxaluria
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Metabolic renal disease\Primary hyperoxaluria
\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
\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
\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
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Primary hyperoxaluria
\Disease\Metabolic disease\Metabolic renal disease\Primary hyperoxaluria
\Disease\Metabolic disease\Enzymopathy\Primary hyperoxaluria
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Primary hyperoxaluria
\Disease\Congenital disease\Inborn error of metabolism\Primary hyperoxaluria

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

30247019 Primary hyperoxaluria en Synonym Active Entire term case insensitive SNOMED CT core module
30248012 Primary hyperoxaluria, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
30249016 Primary oxalosis, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
30250016 Primary oxalosis en Synonym Active Entire term case insensitive SNOMED CT core module
745258015 Primary hyperoxaluria (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
Primary hyperoxaluria	Is a	Hereditary disorder of the urinary system	false	Inferred relationship	Existential restriction modifier
Primary hyperoxaluria	Is a	Inborn error of metabolism	true	Inferred relationship	Existential restriction modifier
Primary hyperoxaluria	Is a	Metabolic renal disease	true	Inferred relationship	Existential restriction modifier
Primary hyperoxaluria	Is a	Disorder of carbohydrate metabolism	true	Inferred relationship	Existential restriction modifier
Primary hyperoxaluria	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Primary hyperoxaluria	Is a	Enzymopathy	true	Inferred relationship	Existential restriction modifier
Primary hyperoxaluria	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Primary hyperoxaluria	Finding site	Kidney structure	true	Inferred relationship	Existential restriction modifier	2
Primary hyperoxaluria	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Primary hyperoxaluria	Is a	Hereditary nephropathy	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Primary hyperoxaluria, type II	Is a	True	Primary hyperoxaluria	Inferred relationship	Existential restriction modifier
Primary hyperoxaluria, type I	Is a	True	Primary hyperoxaluria	Inferred relationship	Existential restriction modifier
[EDTA] Primary oxalosis associated with renal failure	Is a	False	Primary hyperoxaluria	Inferred relationship	Existential restriction modifier
Primary hyperoxaluria type III	Is a	True	Primary hyperoxaluria	Inferred relationship	Existential restriction modifier
Primary hyperoxaluria, type III	Is a	True	Primary hyperoxaluria	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets