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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


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 Some
Iminoglycinuria Is a Specific renal tubule transport defect true Inferred relationship Some
Iminoglycinuria Is a Amino acid transport disorder true Inferred relationship Some
Iminoglycinuria Is a Hereditary disorder of the urinary system false Inferred relationship Some
Iminoglycinuria Occurrence Congenital false Inferred relationship Some
Iminoglycinuria Finding site Kidney structure true Inferred relationship Some 1
Iminoglycinuria Is a Metabolic renal disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Neonatal iminoglycinuria Is a True Iminoglycinuria Inferred relationship Some
Familial renal iminoglycinuria Is a True Iminoglycinuria Inferred relationship Some

This concept is not in any reference sets

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