38795005: Sialidosis (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of movement\Movement disorder\Myoclonic disorder\Sialidosis
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Oligosaccharidosis\Sialidosis
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Sialidosis
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Oligosaccharidosis\Sialidosis
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucolipidosis\Sialidosis
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Sialidosis
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Sialidosis
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Sialidosis
• \Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Sialidosis
• \Disease\Disorder of body system\Disorder of nervous system\Myoclonic disorder\Sialidosis
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Oligosaccharidosis\Sialidosis
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Sialidosis
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Oligosaccharidosis\Sialidosis
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucolipidosis\Sialidosis
• \Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Oligosaccharidosis\Sialidosis
• \Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Mucolipidosis\Sialidosis
• \Disease\Congenital disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Oligosaccharidosis\Sialidosis
• \Disease\Congenital disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Sialidosis
• \Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Oligosaccharidosis\Sialidosis
• \Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucolipidosis\Sialidosis
• \Disease\Movement disorder\Myoclonic disorder\Sialidosis

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
64560011	Sialidosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
64561010	Neuroaminidase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
64562015	Sialidase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
64563013	Mucolipidosis I	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
197386015	Mucolipidosis, type I	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
197387012	Cherry-red-spot myoclonus syndrome	en	Synonym	Inactive	Only initial character case insensitive	SNOMED CT core module
775125012	Sialidosis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1229462014	Cherry-red spot myoclonus syndrome	en	Synonym	Inactive	Only initial character case insensitive	SNOMED CT core module
1229463016	Mucolipidosis type I	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
1229464010	Neuraminidase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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