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84121007: Iminoglycinuria (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
139496018 Iminoglycinuria en Synonym Active Case insensitive SNOMED CT core
139497010 Iminoglycinuria, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
825899010 Iminoglycinuria (disorder) en Fully specified name Active Case insensitive SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Iminoglycinuria Is a Metabolic renal disease true Inferred relationship Some
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

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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