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717766000: Alport syndrome autosomal dominant (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3306956019 Alport syndrome autosomal dominant (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3310200014 Alport syndrome autosomal dominant en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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