Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3447492018 | Autosomal dominant medullary cystic kidney disease with hyperuricemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3447493011 | Autosomal dominant medullary cystic kidney disease with hyperuricaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3447494017 | Medullary cystic kidney disease 2 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3636195014 | Uromodulin related autosomal dominant tubulointerstitial kidney disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3636196010 | UMOD-related autosomal dominant tubulointerstitial kidney disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3636197018 | Uromodulin related autosomal dominant tubulointerstitial kidney disease (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403026016 | A form of autosomal dominant tubulointerstitial kidney disease (ADTKD) due to UMOD mutations that is clinically characterized by bland urinalysis (absence of blood or protein in the urine), chronic kidney disease (CKD) leading to end-stage kidney disease (ESKD) between 20 and 80 years, and gout occurring in 50% of affected individuals. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403027013 | A form of autosomal dominant tubulointerstitial kidney disease (ADTKD) due to UMOD mutations that is clinically characterised by bland urinalysis (absence of blood or protein in the urine), chronic kidney disease (CKD) leading to end-stage kidney disease (ESKD) between 20 and 80 years, and gout occurring in 50% of affected individuals. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3447491013 | Autosomal dominant medullary cystic kidney disease with hyperuricemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3447492018 | Autosomal dominant medullary cystic kidney disease with hyperuricemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3447493011 | Autosomal dominant medullary cystic kidney disease with hyperuricaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3447494017 | Medullary cystic kidney disease 2 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3636195014 | Uromodulin related autosomal dominant tubulointerstitial kidney disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3636196010 | UMOD-related autosomal dominant tubulointerstitial kidney disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3636197018 | Uromodulin related autosomal dominant tubulointerstitial kidney disease (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403026016 | A form of autosomal dominant tubulointerstitial kidney disease (ADTKD) due to UMOD mutations that is clinically characterized by bland urinalysis (absence of blood or protein in the urine), chronic kidney disease (CKD) leading to end-stage kidney disease (ESKD) between 20 and 80 years, and gout occurring in 50% of affected individuals. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403027013 | A form of autosomal dominant tubulointerstitial kidney disease (ADTKD) due to UMOD mutations that is clinically characterised by bland urinalysis (absence of blood or protein in the urine), chronic kidney disease (CKD) leading to end-stage kidney disease (ESKD) between 20 and 80 years, and gout occurring in 50% of affected individuals. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3381611001000118 | Nierenerkrankung, tubulointerstitielle, autosomal-dominante, UMOD-assoziierte | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
888311000172113 | maladie des kystes médullaires rénaux autosomique dominante type 2 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
1010491000172112 | néphropathie tubulo-interstitielle autosomique dominante associée à UMOD | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
888311000172113 | maladie des kystes médullaires rénaux autosomique dominante type 2 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
1010491000172112 | néphropathie tubulo-interstitielle autosomique dominante associée à UMOD | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3381611001000118 | Nierenerkrankung, tubulointerstitielle, autosomal-dominante, UMOD-assoziierte | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
UMOD-related autosomal dominant tubulointerstitial kidney disease | Is a | Autosomal dominant tubulointerstitial kidney disease (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
UMOD-related autosomal dominant tubulointerstitial kidney disease | Associated morphology | Fibrocystic change | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
UMOD-related autosomal dominant tubulointerstitial kidney disease | Finding site | Structure of medulla of kidney | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)