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65524005: Mannosidosis (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
108872013 Mannosidosis en Synonym Active Entire term case insensitive SNOMED CT core module
108874014 alpha-Mannosidase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
805037019 Mannosidosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1232691014 Alpha-D-mannosidosis en Synonym Active Only initial character case insensitive SNOMED CT core module
1232692019 Alpha-mannosidase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mannosidosis Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Mannosidosis Is a Dysostosis multiplex group true Inferred relationship Existential restriction modifier
Mannosidosis Is a Disorder of glycoprotein metabolism false Inferred relationship Existential restriction modifier
Mannosidosis Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Mannosidosis Occurrence Congenital false Inferred relationship Existential restriction modifier
Mannosidosis Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Mannosidosis Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
Mannosidosis Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Mannosidosis Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Mannosidosis Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Mannosidosis Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Mannosidosis Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Mannosidosis Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Mannosidosis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Mannosidosis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Mannosidosis Is a Oligosaccharidosis true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Beta-D-mannosidosis Is a False Mannosidosis Inferred relationship Existential restriction modifier
Mannosidosis, type II Is a True Mannosidosis Inferred relationship Existential restriction modifier
Mannosidosis, type I Is a True Mannosidosis Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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