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65524005: Mannosidosis (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
108872013 Mannosidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
108874014 alpha-Mannosidase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
805037019 Mannosidosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1232691014 Alpha-D-mannosidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1232692019 Alpha-mannosidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
108872013 Mannosidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
108872013 Mannosidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
108874014 alpha-Mannosidase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
805037019 Mannosidosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
805037019 Mannosidosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1232691014 Alpha-D-mannosidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1232692019 Alpha-mannosidase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1232692019 Alpha-mannosidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4604491000241110 mannosidose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4604491000241110 mannosidose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (core metadata concept)
Mannosidosis Is a Dysostosis multiplex group true Inferred relationship Existential restriction modifier (core metadata concept)
Mannosidosis Is a Disorder of glycoprotein metabolism false Inferred relationship Existential restriction modifier (core metadata concept)
Mannosidosis Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Mannosidosis Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Mannosidosis Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Mannosidosis Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Mannosidosis Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Mannosidosis Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Mannosidosis Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Mannosidosis Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Mannosidosis Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Mannosidosis Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Mannosidosis Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Mannosidosis Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Mannosidosis Is a Oligosaccharidosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Mannosidosis Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Mannosidosis Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Beta-D-mannosidosis Is a False Mannosidosis Inferred relationship Existential restriction modifier (core metadata concept)
Mannosidosis, type II Is a True Mannosidosis Inferred relationship Existential restriction modifier (core metadata concept)
Mannosidosis, type I Is a True Mannosidosis Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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