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726017001: Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3447488013 Autosomal dominant medullary cystic kidney disease without hyperuricemia en Synonym Active Entire term case insensitive SNOMED CT core module
3447489017 Autosomal dominant medullary cystic kidney disease without hyperuricaemia en Synonym Active Entire term case insensitive SNOMED CT core module
3447490014 Medullary cystic kidney disease 1 en Synonym Active Entire term case insensitive SNOMED CT core module
3636198011 Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3636199015 MUC1-related autosomal dominant tubulointerstitial kidney disease en Synonym Active Entire term case sensitive SNOMED CT core module
3636200017 Mucin 1 related autosomal dominant tubulointerstitial kidney disease en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mucin 1 related autosomal dominant tubulointerstitial kidney disease Is a Autosomal dominant tubulointerstitial kidney disease true Inferred relationship Existential restriction modifier
Mucin 1 related autosomal dominant tubulointerstitial kidney disease Associated morphology Fibrocystic change true Inferred relationship Existential restriction modifier 1
Mucin 1 related autosomal dominant tubulointerstitial kidney disease Finding site Structure of medulla of kidney true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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