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75652008: Familial renal iminoglycinuria (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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