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 |
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