Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5033755019 | Congenital nephrosis, cerebral ventriculomegaly syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5033756018 | VMCKD - ventriculomegaly with cystic kidney disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5033757010 | Cerebral ventriculomegaly, cystic kidney disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5033758017 | Cerebral ventriculomegaly, cystic kidney disease (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 13605861000146119 | ventriculomegalie en cystenieren | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 13605871000146113 | ventriculomegalie en polycysteuze nierziekte | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 13605881000146110 | syndroom van congenitale nefrose en vergroting van hersenventrikel | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 13605891000146112 | ventriculomegalie en polycysteuze nierziekte (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 5033762011 | A rare genetic syndrome with a central nervous system malformation as a major feature, and characteristics of a triad of high alpha-fetoprotein levels in both maternal serum and amniotic fluid, cerebral ventriculomegaly, renal macro and microcysts. Variable findings include congenital nephrotic syndrome, aqueductal stenosis, gray matter heterotopias and cardiac malformations among others. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5033763018 | A rare genetic syndrome with a central nervous system malformation as a major feature, and characteristics of a triad of high alpha-fetoprotein levels in both maternal serum and amniotic fluid, cerebral ventriculomegaly, renal macro and microcysts. Variable findings include congenital nephrotic syndrome, aqueductal stenosis, grey matter heterotopias and cardiac malformations among others. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cerebral ventriculomegaly, cystic kidney disease | Is a | Congenital cerebral ventriculomegaly (disorder) | true | Inferred relationship | Some | ||
| Cerebral ventriculomegaly, cystic kidney disease | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Cerebral ventriculomegaly, cystic kidney disease | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Cerebral ventriculomegaly, cystic kidney disease | Is a | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
| Cerebral ventriculomegaly, cystic kidney disease | Is a | Congenital cystic kidney disease | true | Inferred relationship | Some | ||
| Cerebral ventriculomegaly, cystic kidney disease | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Cerebral ventriculomegaly, cystic kidney disease | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Cerebral ventriculomegaly, cystic kidney disease | Finding site | Kidney structure | true | Inferred relationship | Some | 1 | |
| Cerebral ventriculomegaly, cystic kidney disease | Associated morphology | Polycystic change | true | Inferred relationship | Some | 1 | |
| Cerebral ventriculomegaly, cystic kidney disease | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Cerebral ventriculomegaly, cystic kidney disease | Finding site | Entire ventricle of brain | true | Inferred relationship | Some | 2 | |
| Cerebral ventriculomegaly, cystic kidney disease | Associated morphology | Enlargement (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
| Cerebral ventriculomegaly, cystic kidney disease | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR