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818952002: Fibronectin glomerulopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3856295011 Fibronectin glomerulopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3856296012 Glomerulopathy with fibronectin deposits en Synonym Active Entire term case insensitive SNOMED CT core module
3856297015 Fibronectin glomerulopathy (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
Fibronectin glomerulopathy Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Fibronectin glomerulopathy Is a Hereditary nephropathy true Inferred relationship Existential restriction modifier
Fibronectin glomerulopathy Is a Renal disorders in inherited disease false Inferred relationship Existential restriction modifier
Fibronectin glomerulopathy Is a Glomerular disease true Inferred relationship Existential restriction modifier
Fibronectin glomerulopathy Finding site Glomerulus structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Glomerulopathy with giant fibrillar deposits Is a True Fibronectin glomerulopathy Inferred relationship Existential restriction modifier
Glomerulopathy with fibronectin deposits 2 Is a True Fibronectin glomerulopathy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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