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

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

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

\Finding of trunk structure\Liver finding\Disease of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\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\Mucopolysaccharidosis\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Genetic disease\Hereditary disease\X-linked recessive hereditary disease\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Fetal and/or neonatal disorder\Congenital disease\Inborn error of metabolism\Storage disease\Mucopolysaccharidosis\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Disorder of body system\Disease of liver\Metabolic and genetic disorder affecting the liver\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form
\Disease\Disorder of trunk (disorder)\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\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\Mucopolysaccharidosis\Mucopolysaccharidosis, MPS-II\Hunter's syndrome, mild form

Status: current. Date: 31-Jan 2002

Descriptions:

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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hunter's syndrome, mild form	Is a	Mucopolysaccharidosis, MPS-II	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Hunter's syndrome, mild form	Occurrence	Congenital	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1
Hunter's syndrome, mild form	Finding site	Liver structure	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	2

Inbound Relationships

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This concept is not in any reference sets