17901006: Primary hyperoxaluria (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Abdominal organ finding\Kidney disease\Primary hyperoxaluria

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Kidney disease\Primary hyperoxaluria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Primary hyperoxaluria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Kidney disease\Primary hyperoxaluria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Kidney disease\Primary hyperoxaluria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disorder of the genitourinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Primary hyperoxaluria
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Kidney disease\Primary hyperoxaluria
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Primary hyperoxaluria

\Disease\Genetic disease\Hereditary disease\Inborn error of metabolism\Primary hyperoxaluria
\Disease\Genetic disease\Hereditary disease\Autosomal recessive hereditary disorder (disorder)\Primary hyperoxaluria
\Disease\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Primary hyperoxaluria
\Disease\Disorder of body system\Disorder of the genitourinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Primary hyperoxaluria
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Kidney disease\Primary hyperoxaluria
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Primary hyperoxaluria
\Disease\Metabolic disease\Inborn error of metabolism\Primary hyperoxaluria
\Disease\Metabolic disease\Enzymopathy\Primary hyperoxaluria
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Primary hyperoxaluria

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: IPS terminology module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

30247019 Primary hyperoxaluria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
30250016 Primary oxalosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
745258015 Primary hyperoxaluria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Primary hyperoxaluria	Is a	Disorder of carbohydrate metabolism	true	Inferred relationship	Some
Primary hyperoxaluria	Is a	Enzymopathy	true	Inferred relationship	Some
Primary hyperoxaluria	Is a	Autosomal recessive hereditary disorder (disorder)	true	Inferred relationship	Some
Primary hyperoxaluria	Is a	Inborn error of metabolism	true	Inferred relationship	Some
Primary hyperoxaluria	Is a	Kidney disease	true	Inferred relationship	Some
Primary hyperoxaluria	Occurrence	Congenital	true	Inferred relationship	Some	1
Primary hyperoxaluria	Finding site	Kidney structure	true	Inferred relationship	Some	2

Inbound Relationships

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Reference Sets

International Patient Summary