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75652008: Familial renal iminoglycinuria (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
125653016 Familial renal iminoglycinuria en Synonym Active Case insensitive SNOMED CT core
816286010 Familial renal iminoglycinuria (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial renal iminoglycinuria Is a Hereditary disorder of the urinary system false Inferred relationship Some
Familial renal iminoglycinuria Is a Inborn error of metabolism true Inferred relationship Some
Familial renal iminoglycinuria Is a Familial disease true Inferred relationship Some
Familial renal iminoglycinuria Is a Iminoglycinuria true Inferred relationship Some
Familial renal iminoglycinuria Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Familial renal iminoglycinuria Is a Hereditary nephropathy true Inferred relationship Some
Familial renal iminoglycinuria Finding site Kidney structure true Inferred relationship Some 2
Familial renal iminoglycinuria Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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