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61598006: Glycogenosis with glucoaminophosphaturia (disorder)


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
102346017 Glycogenosis with glucoaminophosphaturia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
102347014 Fanconi-Bickel syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
102348016 Renal glucose-losing syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
102349012 Pseudo-phlorizin diabetes en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
102350012 Hepatic glycogenosis with de Toni-Debré-Fanconi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
102351011 Hepatic glycogenosis with de Toni-Debre-Fanconi syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
800677014 Glycogenosis with glucoaminophosphaturia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
12745311000172110 syndrome de Fanconi-Bickel fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
12745321000172117 glycogénose avec glucoaminophosphaturie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4950241000172113 GSD type XI nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
4950251000172110 syndroom van Fanconi-Bickel nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
4950261000172112 glycogeenstapelingsziekte type XI nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glycogenosis with glucoaminophosphaturia Is a Hereditary disorder of the urinary system false Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Is a Congenital anomaly of liver true Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Is a Glycogen storage disease true Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Is a Kidney disease false Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Finding site Kidney structure false Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Finding site Digestive organ structure false Inferred relationship Some 1
Glycogenosis with glucoaminophosphaturia Finding site Liver structure false Inferred relationship Some 1
Glycogenosis with glucoaminophosphaturia Finding site Skeletal muscle structure (body structure) false Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Occurrence Congenital false Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Associated morphology Developmental anomaly false Inferred relationship Some 1
Glycogenosis with glucoaminophosphaturia Is a Congenital anomaly of skeletal muscle false Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Finding site Structure of digestive system (body structure) false Inferred relationship Some 1
Glycogenosis with glucoaminophosphaturia Associated morphology Congenital anomaly false Inferred relationship Some 1
Glycogenosis with glucoaminophosphaturia Is a Congenital anomaly of trunk false Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Is a Congenital anomaly of abdomen false Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Is a Congenital anomaly of body cavity false Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Finding site Liver structure false Inferred relationship Some 1
Glycogenosis with glucoaminophosphaturia Associated morphology Congenital anomaly false Inferred relationship Some 1
Glycogenosis with glucoaminophosphaturia Occurrence Congenital true Inferred relationship Some 2
Glycogenosis with glucoaminophosphaturia Associated morphology Developmental anomaly false Inferred relationship Some 2
Glycogenosis with glucoaminophosphaturia Finding site Liver structure true Inferred relationship Some 2
Glycogenosis with glucoaminophosphaturia Is a Hereditary nephropathy (disorder) true Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Finding site Kidney structure true Inferred relationship Some 1
Glycogenosis with glucoaminophosphaturia Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Glycogenosis with glucoaminophosphaturia Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Glycogenosis with glucoaminophosphaturia Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Glycogenosis with glucoaminophosphaturia Occurrence Congenital true Inferred relationship Some 1
Glycogenosis with glucoaminophosphaturia Is a Developmental hereditary disorder true Inferred relationship Some
Glycogenosis with glucoaminophosphaturia Is a Metabolic renal disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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