715864007: Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)

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

\Viscus structure finding (finding)\Liver finding\Disease of liver\...

\Structural abnormality of liver (disorder)\Lesion of liver\Hepatic fibrosis\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Structural abnormality of liver (disorder)\Liver regeneration\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)

\Disorder of liver due to disorder of mineral metabolism (disorder)\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)

\Chronic liver disease\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)

\Finding of trunk structure\Liver finding\Disease of liver\Structural abnormality of liver (disorder)\Lesion of liver\Hepatic fibrosis\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Finding of trunk structure\Liver finding\Disease of liver\Structural abnormality of liver (disorder)\Liver regeneration\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Finding of trunk structure\Liver finding\Disease of liver\Disorder of liver due to disorder of mineral metabolism (disorder)\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Finding of trunk structure\Liver finding\Disease of liver\Chronic liver disease\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\Structural abnormality of liver (disorder)\Lesion of liver\Hepatic fibrosis\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\Structural abnormality of liver (disorder)\Liver regeneration\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\Disorder of liver due to disorder of mineral metabolism (disorder)\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\Chronic liver disease\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)

\Disease\Disorder of body system\Disease of liver\Structural abnormality of liver (disorder)\Lesion of liver\Hepatic fibrosis\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Disease\Disorder of body system\Disease of liver\Structural abnormality of liver (disorder)\Liver regeneration\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Disease\Disorder of body system\Disease of liver\Disorder of liver due to disorder of mineral metabolism (disorder)\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Disease\Disorder of body system\Disease of liver\Chronic liver disease\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Disease\Disorder of trunk (disorder)\Disease of liver\Structural abnormality of liver (disorder)\Lesion of liver\Hepatic fibrosis\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Disease\Disorder of trunk (disorder)\Disease of liver\Structural abnormality of liver (disorder)\Liver regeneration\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Disease\Disorder of trunk (disorder)\Disease of liver\Disorder of liver due to disorder of mineral metabolism (disorder)\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Disease\Disorder of trunk (disorder)\Disease of liver\Chronic liver disease\Cirrhosis of liver\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
\Disease\Idiopathic disease\Cryptogenic cirrhosis\Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)

Status: current. Date: 31-Jul 2016

Descriptions:

Id Description Lang Type Status Case? Module

3303974016 Non-Wilsonian hepatic copper toxicosis of infancy and childhood en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303976019 A rare copper-overload liver disease with rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency. Specific pathological aspects; pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining. en Definition Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
3304658017 Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3304659013 Idiopathic copper associated cirrhosis of liver en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401144015 Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterized by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harboring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401145019 Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterised by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harbouring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining. 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
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	Is a	Disorder of liver due to disorder of mineral metabolism (disorder)	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	Is a	Cryptogenic cirrhosis	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	Associated morphology	Chronic fibrosis	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	Finding site	Liver structure	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	Associated morphology	Nodular regeneration	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	2
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	Finding site	Liver structure	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	2
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	Occurrence	Childhood	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	3
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	Occurrence	Infancy	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	4
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	Clinical course	Progressive	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	5
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	Due to	Disorder of copper metabolism	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	6

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3303974016	Non-Wilsonian hepatic copper toxicosis of infancy and childhood	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3303976019	A rare copper-overload liver disease with rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency. Specific pathological aspects; pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining.	en	Definition	Inactive	Entire term case sensitive (core metadata concept)	SNOMED CT core
3304658017	Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3304659013	Idiopathic copper associated cirrhosis of liver	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5401144015	Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterized by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harboring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401145019	Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterised by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harbouring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core