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38795005: Sialidosis (disorder)


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
775125012 Sialidosis (disorder) en Fully specified name Active Entire term 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


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sialidosis Is a Disorder of glycoprotein metabolism false Inferred relationship Existential restriction modifier
Sialidosis Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier
Sialidosis Is a Lipid storage disease false Inferred relationship Existential restriction modifier
Sialidosis Is a Mucolipidosis true Inferred relationship Existential restriction modifier
Sialidosis Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Sialidosis Is a Inherited metabolic disorder of nervous system true Inferred relationship Existential restriction modifier
Sialidosis Is a Myoclonic disorder true Inferred relationship Existential restriction modifier
Sialidosis Finding site Brain structure false Inferred relationship Existential restriction modifier
Sialidosis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Sialidosis Finding site Structure of muscle tissue false Inferred relationship Existential restriction modifier
Sialidosis Finding site Skeletal and/or smooth muscle structure false Inferred relationship Existential restriction modifier
Sialidosis Finding site Structure of nervous system true Inferred relationship Existential restriction modifier 2
Sialidosis Is a Oligosaccharidosis true Inferred relationship Existential restriction modifier
Sialidosis Interprets Movement true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Normosomatic sialidosis Is a False Sialidosis Inferred relationship Existential restriction modifier
Combined deficiency of sialidase AND beta galactosidase Is a False Sialidosis Inferred relationship Existential restriction modifier
Dysmorphic sialidosis Is a True Sialidosis Inferred relationship Existential restriction modifier
Sialidosis type 1 Is a True Sialidosis Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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