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717768004: Alport syndrome X-linked (disorder)


Status: current, Primitive. 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 Case sensitive SNOMED CT core
3312599010 Alport syndrome X-linked en Synonym Active Case sensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


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

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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