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22751000146108: congenitaal nefrotisch syndroom WT1 mutatie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2017. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module
194381000146112 Congenital nephrotic syndrome due to WT-1 mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
194391000146114 Congenital nephrotic syndrome due to WT-1 mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
712311000146118 congenitaal nefrotisch syndroom WT1 mutatie (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
712321000146111 congenitaal nefrotisch syndroom WT1 mutatie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Is a Congenital nephrotic syndrome true Inferred relationship Some
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Due to Genetic mutation true Inferred relationship Some 4
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Occurrence Congenital false Inferred relationship Some 2
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Finding site Glomerulus structure false Inferred relationship Some 2
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Interprets Measurement of protein in urine (procedure) true Inferred relationship Some 3
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Has interpretation Below reference range true Inferred relationship Some 2
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Finding site Glomerulus structure true Inferred relationship Some 1
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Interprets Albumin measurement true Inferred relationship Some 2
Congenital nephrotic syndrome due to WT-1 mutation (disorder) Has interpretation Above reference range true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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