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717768004: Alport syndrome X-linked (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3311845012 Alport syndrome X-linked (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312599010 Alport syndrome X-linked en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Alport syndrome X-linked (disorder) Is a X-linked hereditary disease false Inferred relationship Some
Alport syndrome X-linked (disorder) Is a Hereditary nephritis (disorder) false Inferred relationship Some
Alport syndrome X-linked (disorder) Associated morphology Chronic inflammation true Inferred relationship Some 1
Alport syndrome X-linked (disorder) Finding site Glomerulus structure true Inferred relationship Some 1
Alport syndrome X-linked (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Some 3
Alport syndrome X-linked (disorder) Is a Alport syndrome (disorder) true Inferred relationship Some
Alport syndrome X-linked (disorder) Interprets Hearing true Inferred relationship Some 2
Alport syndrome X-linked (disorder) Is a X-linked dominant hereditary disease (disorder) true Inferred relationship Some
Alport syndrome X-linked (disorder) Has interpretation Impaired true Inferred relationship Some 2
Alport syndrome X-linked (disorder) Is a X-linked sensorineural hearing loss true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
X-linked diffuse leiomyomatosis with Alport syndrome (disorder) Is a True Alport syndrome X-linked (disorder) Inferred relationship Some

This concept is not in any reference sets

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