5667009: Hunter's syndrome, mild form (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis type II\Hunter's syndrome, mild form

\Digestive system finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis type II\Hunter's syndrome, mild form

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis type II\Hunter's syndrome, mild form

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Disease\Metabolic disease\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Mucopolysaccharidosis type II\Hunter's syndrome, mild form
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Mucopolysaccharidosis type II\Hunter's syndrome, mild form

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

Descriptions:

Id Description Lang Type Status Case? Module

10446017 Hunter's syndrome, mild form en Synonym Active Entire term case sensitive SNOMED CT core module

497670016 Mucopolysaccharidosis type II mild form en Synonym Active Only initial character case insensitive SNOMED CT core module

795208011 Hunter's syndrome, mild form (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

2839084018 Hunter syndrome, mild form en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hunter's syndrome, mild form	Is a	Mucopolysaccharidosis type II	true	Inferred relationship	Existential restriction modifier
Hunter's syndrome, mild form	Finding site	Liver structure	true	Inferred relationship	Existential restriction modifier	2
Hunter's syndrome, mild form	Severity	Mild	false	Inferred relationship	Existential restriction modifier
Hunter's syndrome, mild form	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
10446017	Hunter's syndrome, mild form	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
497670016	Mucopolysaccharidosis type II mild form	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
795208011	Hunter's syndrome, mild form (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
2839084018	Hunter syndrome, mild form	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module