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717767009: Alport syndrome autosomal recessive (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3310202018 Alport syndrome autosomal recessive (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3312046012 Alport syndrome autosomal recessive en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Unit of use quantity reference set

Description inactivation indicator reference set

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