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84121007: Iminoglycinuria (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
139496018 Iminoglycinuria en Synonym Active Entire term case insensitive SNOMED CT core module
139497010 Iminoglycinuria, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
825899010 Iminoglycinuria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core 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
Iminoglycinuria Is a Specific renal tubule transport defect true Inferred relationship Existential restriction modifier
Iminoglycinuria Is a Amino acid transport disorder true Inferred relationship Existential restriction modifier
Iminoglycinuria Is a Hereditary disorder of the urinary system false Inferred relationship Existential restriction modifier
Iminoglycinuria Occurrence Congenital false Inferred relationship Existential restriction modifier
Iminoglycinuria Finding site Kidney structure true Inferred relationship Existential restriction modifier 1
Iminoglycinuria Is a Metabolic renal disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Neonatal iminoglycinuria Is a True Iminoglycinuria Inferred relationship Existential restriction modifier
Familial renal iminoglycinuria Is a True Iminoglycinuria Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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