40951006: Primary hyperoxaluria, type II (disorder)

SNOMED CT Concept\constatation clinique\...

\Viscus structure finding (finding)\constatation à propos d'un organe abdominal\Kidney finding\Kidney disease\...

\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)

\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)

\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\constatation à propos d'un organe abdominal\Kidney finding\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\constatation à propos d'un organe abdominal\Kidney finding\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Urinary system finding\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Urinary system finding\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Urinary system finding\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\Genetic disease\maladie héréditaire\Inborn error of metabolism\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\affection d'un système corporel\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\affection d'un système corporel\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\affection d'un système corporel\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\Disorder of retroperitoneal compartment (disorder)\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Disorder of kidney and/or ureter (disorder)\Kidney disease\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\trouble de l'appareil génito-urinaire\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\trouble métabolique\maladie métabolique du rein\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\trouble métabolique\Inborn error of metabolism\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\trouble métabolique\Enzymopathy\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\trouble métabolique\Disorder of carbohydrate metabolism\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)
\Disease\Congenital disease\Inborn error of metabolism\Primary hyperoxaluria\hyperoxalurie primitive type 2 (trouble)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

426571000241117 hyperoxalurie primitive type 2 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

492842013 Deficiency of glyoxylate reductase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

492843015 Deficiency of glycerate dehydrogenase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

492844014 Oxalosis type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

492845010 Primary hyperoxaluria type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

68304013 Primary hyperoxaluria, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

68305014 Glyoxylate reductase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

68306010 Glyceric dehydrogenase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

68307018 L-glyceric aciduria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

68308011 Glycerate dehydrogenase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

777685010 Primary hyperoxaluria, type II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

897311000172113 hyperoxalurie primitive type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

903961000172111 acidurie L-glycérique fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
hyperoxalurie primitive type 2 (trouble)	est un(e) (attribut)	Primary hyperoxaluria	true	Inferred relationship	Some
hyperoxalurie primitive type 2 (trouble)	localisation d'une constatation (attribut)	structure d'un rein	true	Inferred relationship	Some	2
hyperoxalurie primitive type 2 (trouble)	survenue (attribut)	congénital	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set