FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

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
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

Back to Start