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723373006: Uromodulin related autosomal dominant tubulointerstitial kidney disease (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3447492018 Autosomal dominant medullary cystic kidney disease with hyperuricemia en Synonym Active Case insensitive SNOMED CT core
3447493011 Autosomal dominant medullary cystic kidney disease with hyperuricaemia en Synonym Active Case insensitive SNOMED CT core
3447494017 Medullary cystic kidney disease 2 en Synonym Active Case insensitive SNOMED CT core
3636195014 Uromodulin related autosomal dominant tubulointerstitial kidney disease en Synonym Active Case insensitive SNOMED CT core
3636196010 UMOD-related autosomal dominant tubulointerstitial kidney disease en Synonym Active Case sensitive SNOMED CT core
3636197018 Uromodulin related autosomal dominant tubulointerstitial kidney disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant medullary cystic kidney disease with hyperuricaemia Is a Autosomal dominant tubulointerstitial kidney disease true Inferred relationship Some
Autosomal dominant medullary cystic kidney disease with hyperuricaemia Associated morphology Fibrocystic change true Inferred relationship Some 1
Autosomal dominant medullary cystic kidney disease with hyperuricaemia Finding site Structure of medulla of kidney true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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