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717459000: Congenital primary megaureter (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5401577013 A rare non-syndromic urogenital tract malformation characterized by a dilated ureter and normal bladder and bladder outlet. It may be obstructed, refluxing or unobstructed and not refluxing. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401578015 A rare non-syndromic urogenital tract malformation characterised by a dilated ureter and normal bladder and bladder outlet. It may be obstructed, refluxing or unobstructed and not refluxing. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3309412012 Congenital primary megaureter (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3309413019 Congenital primary megaureter en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3309414013 Congenital primary megalo-ureter en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1019221000172115 méga-uretère primitif congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3417151001000114 Megaureter, kongenitaler primärer de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare non-syndromic urogenital tract malformation characterized by a dilated ureter and normal bladder and bladder outlet. It may be obstructed, refluxing or unobstructed and not refluxing. Is a Idiopathic dilation of ureter true Inferred relationship Some
A rare non-syndromic urogenital tract malformation characterized by a dilated ureter and normal bladder and bladder outlet. It may be obstructed, refluxing or unobstructed and not refluxing. Is a Congenital dilatation of ureter (disorder) true Inferred relationship Some
A rare non-syndromic urogenital tract malformation characterized by a dilated ureter and normal bladder and bladder outlet. It may be obstructed, refluxing or unobstructed and not refluxing. Associated morphology Congenital dilatation false Inferred relationship Some 1
A rare non-syndromic urogenital tract malformation characterized by a dilated ureter and normal bladder and bladder outlet. It may be obstructed, refluxing or unobstructed and not refluxing. Occurrence Congenital true Inferred relationship Some 1
A rare non-syndromic urogenital tract malformation characterized by a dilated ureter and normal bladder and bladder outlet. It may be obstructed, refluxing or unobstructed and not refluxing. Finding site Ureteric structure true Inferred relationship Some 1
A rare non-syndromic urogenital tract malformation characterized by a dilated ureter and normal bladder and bladder outlet. It may be obstructed, refluxing or unobstructed and not refluxing. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
A rare non-syndromic urogenital tract malformation characterized by a dilated ureter and normal bladder and bladder outlet. It may be obstructed, refluxing or unobstructed and not refluxing. Associated morphology Dilatation true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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