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722369003: Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3331711016 Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331712011 Congenital nephrotic syndrome due to diffuse mesangial sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331713018 Congenital nephrotic syndrome (CNS) due to diffuse mesangial sclerosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3331714012 Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3331711016 Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3331711016 Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331712011 Congenital nephrotic syndrome due to diffuse mesangial sclerosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3331712011 Congenital nephrotic syndrome due to diffuse mesangial sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331713018 Congenital nephrotic syndrome (CNS) due to diffuse mesangial sclerosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3331714012 Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5905241000241113 syndrome néphrotique congénital dû à une sclérose mésangiale diffuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5905251000241111 syndrome néphrotique congénital dû à une sclérose diffuse du mésangium fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5905241000241113 syndrome néphrotique congénital dû à une sclérose mésangiale diffuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5905251000241111 syndrome néphrotique congénital dû à une sclérose diffuse du mésangium fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Due to Diffuse mesangial sclerosis true Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Is a Congenital nephrotic syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Is a Nephrotic syndrome associated with another disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Finding site Glomerulus structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Is a Hereditary nephropathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Interprets Albumin measurement (procedure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Interprets Measurement of protein in urine (procedure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Is a Glomerular disease due to diffuse mesangial sclerosis true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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