FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

717766000: Alport syndrome autosomal dominant (disorder)


Status: current, Primitive. 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 Case sensitive SNOMED CT core
3310200014 Alport syndrome autosomal dominant en Synonym Active Case sensitive SNOMED CT core


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 Some
Alport syndrome autosomal dominant Is a Hereditary nephritis false Inferred relationship Some
Alport syndrome autosomal dominant Associated morphology Chronic inflammation true Inferred relationship Some 1
Alport syndrome autosomal dominant Finding site Glomerulus structure true Inferred relationship Some 1
Alport syndrome autosomal dominant Interprets Hearing true Inferred relationship Some 2
Alport syndrome autosomal dominant Is a Alport syndrome true Inferred relationship Some
Alport syndrome autosomal dominant Finding site Structure of auditory system true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start