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726017001: Mucin 1 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
3447488013 Autosomal dominant medullary cystic kidney disease without hyperuricemia en Synonym Active Case insensitive SNOMED CT core
3447489017 Autosomal dominant medullary cystic kidney disease without hyperuricaemia en Synonym Active Case insensitive SNOMED CT core
3447490014 Medullary cystic kidney disease 1 en Synonym Active Case insensitive SNOMED CT core
3636198011 Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3636199015 MUC1-related autosomal dominant tubulointerstitial kidney disease en Synonym Active Case sensitive SNOMED CT core
3636200017 Mucin 1 related autosomal dominant tubulointerstitial kidney disease en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
MUC1-related autosomal dominant tubulointerstitial kidney disease Is a Autosomal dominant tubulointerstitial kidney disease true Inferred relationship Some
MUC1-related autosomal dominant tubulointerstitial kidney disease Associated morphology Fibrocystic change true Inferred relationship Some 1
MUC1-related autosomal dominant tubulointerstitial kidney disease 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

Description inactivation indicator reference set

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