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

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Liver finding\Liver disease\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form

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

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

10446017 Hunter's syndrome, mild form en Synonym Active Case sensitive SNOMED CT core
2839084018 Hunter syndrome, mild form en Synonym Active Case sensitive SNOMED CT core
497670016 Mucopolysaccharidosis type II mild form en Synonym Active Initial character case insensitive SNOMED CT core
795208011 Hunter's syndrome, mild form (disorder) en Fully specified name Active Case sensitive SNOMED CT core

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

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