237965005: Phosphate transport defect (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Phosphate transport defect

\Disorder of foetus and/or newborn\Congenital disease (disorder)\Inborn error of metabolism\Storage disease\Glycogen storage disease\Phosphate transport defect

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Phosphate transport defect
\Metabolic disease\Disorder of carbohydrate metabolism\Glycogen storage disease\Phosphate transport defect

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

356653011 Glycogen storage disease type Ic en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356654017 Phosphate transport defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626776012 Phosphate transport defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Phosphate transport defect	Is a	Glycogen storage disease	true	Inferred relationship	Some
Phosphate transport defect	Occurrence	Congenital	true	Inferred relationship	Some	1
Phosphate transport defect	Finding site	Liver structure	false	Inferred relationship	Some
Phosphate transport defect	Finding site	Skeletal muscle structure	false	Inferred relationship	Some
Phosphate transport defect	Finding site	Body system structure	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

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This concept is not in any reference sets