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197601003: Finnish congenital nephrotic syndrome (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
303840010 Finnish congenital nephrotic syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
303841014 CNF - Finnish congenital nephrotic syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
303842019 Congenital Finnish nephrosis en Synonym Active Only initial character case insensitive SNOMED CT core module
581998015 Finnish congenital nephrotic syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Finnish congenital nephrotic syndrome Is a Congenital nephrotic syndrome true Inferred relationship Existential restriction modifier
Finnish congenital nephrotic syndrome Finding site Glomerulus structure false Inferred relationship Existential restriction modifier 1
Finnish congenital nephrotic syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Finnish congenital nephrotic syndrome Finding site Urinary system structure false Inferred relationship Existential restriction modifier 4
Finnish congenital nephrotic syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Finnish congenital nephrotic syndrome Course Multiple superficial injuries of lower leg false Inferred relationship Existential restriction modifier
Finnish congenital nephrotic syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Finnish congenital nephrotic syndrome Finding site Glomerulus structure true Inferred relationship Existential restriction modifier 1
Finnish congenital nephrotic syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Finnish congenital nephrotic syndrome Finding site Glomerulus structure false Inferred relationship Existential restriction modifier 2
Finnish congenital nephrotic syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Finnish congenital nephrotic syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Finnish congenital nephrotic syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Finnish congenital nephrotic syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Finnish congenital nephrotic syndrome Interprets Albumin measurement true Inferred relationship Existential restriction modifier 2
Finnish congenital nephrotic syndrome Interprets Measurement of protein in urine true Inferred relationship Existential restriction modifier 3
Finnish congenital nephrotic syndrome Has interpretation Above reference range true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Disorder of glomerulus due to Finnish type congenital nephrotic syndrome Due to True Finnish congenital nephrotic syndrome Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

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