73146005: Hunter's syndrome, severe 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, severe form

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

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

Descriptions:

Id Description Lang Type Status Case? Module

121485018 Hunter's syndrome, severe form en Synonym Active Case sensitive SNOMED CT core
2842547012 Hunter syndrome, severe form en Synonym Active Case sensitive SNOMED CT core
502364017 Mucopolysaccharidosis type II severe form en Synonym Active Initial character case insensitive SNOMED CT core
813502019 Hunter's syndrome, severe 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, severe form	Is a	Mucopolysaccharidosis, MPS-II	true	Inferred relationship	Some
Hunter's syndrome, severe form	Severity	Severe	false	Inferred relationship	Some
Hunter's syndrome, severe form	Finding site	Liver structure	true	Inferred relationship	Some	2
Hunter's syndrome, severe 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
121485018	Hunter's syndrome, severe form	en	Synonym	Active	Case sensitive	SNOMED CT core
2842547012	Hunter syndrome, severe form	en	Synonym	Active	Case sensitive	SNOMED CT core
502364017	Mucopolysaccharidosis type II severe form	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
813502019	Hunter's syndrome, severe form (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core