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235908005: Glycogen storage disease type IX (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
353637017 Glycogen phosphorylase kinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
353639019 PHK - Hepatic phosphorylase kinase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
353640017 Hepatic phosphorylase kinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
353641018 Phosphorylase kinase deficiency of liver en Synonym Active Entire term case insensitive SNOMED CT core module
353642013 Glycogen storage disease type IX en Synonym Active Only initial character case insensitive SNOMED CT core module
353643015 Glycogenosis viiia en Synonym Active Entire term case insensitive SNOMED CT core module
3441358013 Glycogen storage disease type IX (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glycogen storage disease type IX Is a Glycogen storage disease true Inferred relationship Existential restriction modifier
Glycogen storage disease type IX Occurrence Congenital false Inferred relationship Existential restriction modifier
Glycogen storage disease type IX Finding site Liver structure false Inferred relationship Existential restriction modifier
Glycogen storage disease type IX Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier
Glycogen storage disease type IX Finding site Body system structure false Inferred relationship Existential restriction modifier
Glycogen storage disease type IX Is a Disorder of liver true Inferred relationship Existential restriction modifier
Glycogen storage disease type IX Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Glycogen storage disease type IX Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Glycogen storage disease type IX Finding site Liver structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Glycogen phosphorylase kinase deficiency, X-linked Is a False Glycogen storage disease type IX Inferred relationship Existential restriction modifier
Glycogen phosphorylase kinase deficiency, autosomal recessive Is a True Glycogen storage disease type IX Inferred relationship Existential restriction modifier
Glycogen storage disease due to muscle phosphorylase kinase deficiency Is a True Glycogen storage disease type IX Inferred relationship Existential restriction modifier
Glycogen storage disease type IXB Is a True Glycogen storage disease type IX Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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