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15978003: Glycogen storage disease, muscular form (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
27053017 Glycogen storage disease, muscular form en Synonym Active Entire term case insensitive SNOMED CT core module
742910014 Glycogen storage disease, muscular form (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glycogen storage disease, muscular form Is a Glycogen storage disease true Inferred relationship Existential restriction modifier
Glycogen storage disease, muscular form Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 2
Glycogen storage disease, muscular form Finding site Liver structure false Inferred relationship Existential restriction modifier
Glycogen storage disease, muscular form Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Glycogen storage disease, muscular form Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Glycogen storage disease, muscular form Is a Metabolic myopathy true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Glycogen storage disease, type IV Is a True Glycogen storage disease, muscular form Inferred relationship Existential restriction modifier
Glycogen storage disease, type II Is a False Glycogen storage disease, muscular form Inferred relationship Existential restriction modifier
Glycogen storage disease, type V Is a True Glycogen storage disease, muscular form Inferred relationship Existential restriction modifier
Glycogen storage disease, type III Is a True Glycogen storage disease, muscular form Inferred relationship Existential restriction modifier
Glycogen storage disease, type VII Is a True Glycogen storage disease, muscular form Inferred relationship Existential restriction modifier
Equine polysaccharide storage myopathy Is a False Glycogen storage disease, muscular form Inferred relationship Existential restriction modifier
Glycogen storage disease due to muscle beta-enolase deficiency Is a True Glycogen storage disease, muscular form Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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