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717766000: Alport syndrome autosomal dominant (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
3306956019 Alport syndrome autosomal dominant (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3310200014 Alport syndrome autosomal dominant en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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