62216007: Familial arthrogryposis-cholestatic hepatorenal syndrome (disorder)

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

\Viscus structure finding (finding)\Liver finding\Disease of liver\Hepatic failure\Hepatorenal syndrome\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Viscus structure finding (finding)\Renal failure syndrome\Hepatorenal syndrome\Familial arthrogryposis-cholestatic hepatorenal syndrome

\Finding of trunk structure\Liver finding\Disease of liver\Hepatic failure\Hepatorenal syndrome\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\Hepatic failure\Hepatorenal syndrome\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Finding of trunk structure\Disorder of trunk (disorder)\Renal failure syndrome\Hepatorenal syndrome\Familial arthrogryposis-cholestatic hepatorenal syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of bilirubin metabolism\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Disease\Fetal and/or neonatal disorder\Congenital disease\Inborn error of metabolism\Inherited disorder of bilirubin metabolism\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Disease\Disorder of body system\Disease of liver\Hepatic failure\Hepatorenal syndrome\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Disease\Disorder of body system\Renal failure syndrome\Hepatorenal syndrome\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Disease\Disorder of trunk (disorder)\Disease of liver\Hepatic failure\Hepatorenal syndrome\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Disease\Disorder of trunk (disorder)\Renal failure syndrome\Hepatorenal syndrome\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Disease\Familial disease\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of bilirubin metabolism\Familial arthrogryposis-cholestatic hepatorenal syndrome
\Disease\Metabolic disease\Disorder of bilirubin metabolism\Inherited disorder of bilirubin metabolism\Familial arthrogryposis-cholestatic hepatorenal syndrome

Status: current. Date: 31-Jul 2002

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial arthrogryposis-cholestatic hepatorenal syndrome	Is a	Familial disease	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Familial arthrogryposis-cholestatic hepatorenal syndrome	Is a	Hepatorenal syndrome	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Familial arthrogryposis-cholestatic hepatorenal syndrome	Is a	Inherited disorder of bilirubin metabolism	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Familial arthrogryposis-cholestatic hepatorenal syndrome	Associated morphology	Contracture	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1
Familial arthrogryposis-cholestatic hepatorenal syndrome	Occurrence	Congenital	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1
Familial arthrogryposis-cholestatic hepatorenal syndrome	Finding site	Structure of joint region	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1
Familial arthrogryposis-cholestatic hepatorenal syndrome	Pathological process (attribute)	Pathological developmental process	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1
Familial arthrogryposis-cholestatic hepatorenal syndrome	Associated morphology	Contracture	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	2
Familial arthrogryposis-cholestatic hepatorenal syndrome	Finding site	Joint structure of multiple body sites (body structure)	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	2
Familial arthrogryposis-cholestatic hepatorenal syndrome	Has interpretation	Decreased	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	3
Familial arthrogryposis-cholestatic hepatorenal syndrome	Interprets	Range of joint movement	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	3
Familial arthrogryposis-cholestatic hepatorenal syndrome	Has interpretation	Impaired	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	4
Familial arthrogryposis-cholestatic hepatorenal syndrome	Interprets	Renal function	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	4
Familial arthrogryposis-cholestatic hepatorenal syndrome	Finding site	Liver structure	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	5
Familial arthrogryposis-cholestatic hepatorenal syndrome	Finding site	Kidney structure	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	6

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

US English

Congenital syphilitic hepatomegaly

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Id	Description	Lang	Type	Status	Case?	Module
103394013	Familial arthrogryposis-cholestatic hepatorenal syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
103395014	Lethal familial cholestatic and pigmentary liver disease	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
103396010	Lethal familial cholestatic AND pigmentary liver disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
499227017	Familial arthrogryposis - cholestatic hepatorenal syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
801364018	Familial arthrogryposis-cholestatic hepatorenal syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core