40191005: Glycogen storage disease, type IX (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

63817015 Glycogen storage disease, type IX en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

776788013 Glycogen storage disease, type IX (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3035493014 Glycogen storage disease type 9 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

63817015 Glycogen storage disease, type IX en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

63818013 Hepatic glycogen phosphorylase kinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

63819017 GSD IX en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

776788013 Glycogen storage disease, type IX (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3035493014 Glycogen storage disease type 9 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3035493014 Glycogen storage disease type 9 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glycogen storage disease, type IX	Is a	Glycogen storage disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Glycogen storage disease, type IX	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Glycogen storage disease, type IX	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Glycogen storage disease, type IX	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Glycogen storage disease, type IX	Is a	Glycogen storage disease, hepatic form	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

SAME AS association reference set (foundation metadata concept)