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1197417009: Congenital portosystemic shunt (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4696263014 Congenital portosystemic shunt (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4696264015 Congenital portosystemic venous fistula en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4696265019 Congenital portosystemic shunt en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4696266018 A rare congenital anomaly of the great veins characterised by an abnormal communication between one or more veins of the portal and the caval systems, resulting in complete or partial diversion of the portal blood away from the liver to the systemic circulation. Clinical manifestations include liver atrophy, hypergalactosaemia without uridine diphosphate enzyme deficiency, hyperammonaemia, encephalopathy (resulting in learning disabilities, extreme fatigability and seizures), pulmonary hypertension, hypoxaemia from hepatopulmonary syndrome and benign or malignant tumours. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

4696267010 A rare congenital anomaly of the great veins characterized by an abnormal communication between one or more veins of the portal and the caval systems, resulting in complete or partial diversion of the portal blood away from the liver to the systemic circulation. Clinical manifestations include liver atrophy, hypergalactosemia without uridine diphosphate enzyme deficiency, hyperammonemia, encephalopathy (resulting in learning disabilities, extreme fatigability and seizures), pulmonary hypertension, hypoxemia from hepatopulmonary syndrome and benign or malignant tumors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital portosystemic shunt	Is a	Disorder of portal venous system	false	Inferred relationship	Some
Congenital portosystemic shunt	Is a	Anomalies of great veins	false	Inferred relationship	Some
Congenital portosystemic shunt	Is a	Congenital abnormality of vein	false	Inferred relationship	Some
Congenital portosystemic shunt	Is a	Congenital anomaly of abdomen	false	Inferred relationship	Some
Congenital portosystemic shunt	Is a	Congenital anomaly of cardiovascular structure of trunk	false	Inferred relationship	Some
Congenital portosystemic shunt	Occurrence	Congenital	false	Inferred relationship	Some	1
Congenital portosystemic shunt	Finding site	Structure of great vein (body structure)	false	Inferred relationship	Some	1
Congenital portosystemic shunt	Associated morphology	Abnormal communication	false	Inferred relationship	Some	1
Congenital portosystemic shunt	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	1
Congenital portosystemic shunt	Occurrence	Congenital	false	Inferred relationship	Some	2
Congenital portosystemic shunt	Finding site	Portal venous system structure	false	Inferred relationship	Some	2
Congenital portosystemic shunt	Associated morphology	Abnormal communication	false	Inferred relationship	Some	2
Congenital portosystemic shunt	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
4696263014	Congenital portosystemic shunt (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4696264015	Congenital portosystemic venous fistula	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4696265019	Congenital portosystemic shunt	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4696266018	A rare congenital anomaly of the great veins characterised by an abnormal communication between one or more veins of the portal and the caval systems, resulting in complete or partial diversion of the portal blood away from the liver to the systemic circulation. Clinical manifestations include liver atrophy, hypergalactosaemia without uridine diphosphate enzyme deficiency, hyperammonaemia, encephalopathy (resulting in learning disabilities, extreme fatigability and seizures), pulmonary hypertension, hypoxaemia from hepatopulmonary syndrome and benign or malignant tumours.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4696267010	A rare congenital anomaly of the great veins characterized by an abnormal communication between one or more veins of the portal and the caval systems, resulting in complete or partial diversion of the portal blood away from the liver to the systemic circulation. Clinical manifestations include liver atrophy, hypergalactosemia without uridine diphosphate enzyme deficiency, hyperammonemia, encephalopathy (resulting in learning disabilities, extreme fatigability and seizures), pulmonary hypertension, hypoxemia from hepatopulmonary syndrome and benign or malignant tumors.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core