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770414008: Alport syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3700751016 Alport syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3700752011 Alport syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404782017 A rare renal disease characterized by glomerular nephropathy with hematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404783010 A rare renal disease characterised by glomerular nephropathy with haematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Alport syndrome (disorder) Associated morphology Chronic inflammation false Inferred relationship Some 1
Alport syndrome (disorder) Interprets Hearing true Inferred relationship Some 3
Alport syndrome (disorder) Is a Hereditary nephritis (disorder) true Inferred relationship Some
Alport syndrome (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Some 2
Alport syndrome (disorder) Finding site Glomerulus structure true Inferred relationship Some 1
Alport syndrome (disorder) Is a Sensorineural hearing loss true Inferred relationship Some
Alport syndrome (disorder) Is a Auditory system hereditary disorder true Inferred relationship Some
Alport syndrome (disorder) Associated morphology Chronic inflammatory morphology (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Alport syndrome autosomal recessive (disorder) Is a True Alport syndrome (disorder) Inferred relationship Some
Alport syndrome X-linked (disorder) Is a True Alport syndrome (disorder) Inferred relationship Some
Alport syndrome autosomal dominant (disorder) Is a True Alport syndrome (disorder) Inferred relationship Some
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) Is a False Alport syndrome (disorder) Inferred relationship Some
Glomerular disease due to Alport syndrome Due to True Alport syndrome (disorder) Inferred relationship Some 2

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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