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84121007: Iminoglycinuria (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
139496018 Iminoglycinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
825899010 Iminoglycinuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
139496018 Iminoglycinuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
139496018 Iminoglycinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
825899010 Iminoglycinuria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
825899010 Iminoglycinuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3430441001000112 Iminoglycinurie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
925651000172111 iminoglycinurie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
925651000172111 iminoglycinurie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3430441001000112 Iminoglycinurie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Iminoglycinuria Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
Iminoglycinuria Is a Specific renal tubule transport defect (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Iminoglycinuria Is a Amino acid transport disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Iminoglycinuria Is a Hereditary disorder of the urinary system false Inferred relationship Existential restriction modifier (core metadata concept)
Iminoglycinuria Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Iminoglycinuria Finding site Kidney structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Iminoglycinuria Is a Metabolic renal disease true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Neonatal iminoglycinuria Is a True Iminoglycinuria Inferred relationship Existential restriction modifier (core metadata concept)
Familial renal iminoglycinuria Is a True Iminoglycinuria Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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