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5667009: lichte vorm van mucopolysacharidose type II (aandoening)

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

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

\Digestive system finding (finding)\Liver finding\Disease of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Digestive system hereditary disorder (disorder)\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Lysosomal storage disease (disorder)\Mucopolysaccharidosis\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder (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 foetus and/or newborn\Congenital disease (disorder)\Inborn error of metabolism\Storage disease\Lysosomal storage disease (disorder)\Mucopolysaccharidosis\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Disorder of foetus and/or newborn\Disorder of digestive system specific to fetus OR newborn\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder (disorder)\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Digestive system hereditary disorder (disorder)\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of liver and/or biliary tract\Disease of liver\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\Lysosomal storage disease (disorder)\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\Lysosomal storage disease (disorder)\Mucopolysaccharidosis\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

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

Descriptions:

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

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
10446017	Hunter's syndrome, mild form	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
497670016	Mucopolysaccharidosis type II mild form	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
795208011	Hunter's syndrome, mild form (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2839084018	Hunter syndrome, mild form	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
6136051000146117	lichte vorm van mucopolysacharidose type II (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6889951000146112	lichte vorm van MPS II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6889961000146110	lichte vorm van mucopolysacharidose type II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6889971000146116	lichte vorm van mucopolysacharidose type 2B	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6889981000146119	lichte vorm van iduronaat 2-sulfatasedeficiëntie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6889991000146117	lichte vorm van sulfoïduronaatsulfatasedeficiëntie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6890001000146118	lichte vorm van syndroom van Hunter	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)