Status: current, Primitive. Date: 30-Apr 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5033755019 | Congenital nephrosis, cerebral ventriculomegaly syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
5033756018 | VMCKD - ventriculomegaly with cystic kidney disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
5033757010 | Cerebral ventriculomegaly, cystic kidney disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
5033758017 | Cerebral ventriculomegaly, cystic kidney disease (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
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 | Case sensitive | 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 | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Cerebral ventriculomegaly, cystic kidney disease | Is a | Congenital cerebral ventriculomegaly | 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 | true | Inferred relationship | Some | ||
Cerebral ventriculomegaly, cystic kidney disease | Is a | Polycystic 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 | true | Inferred relationship | Some | 2 | |
Cerebral ventriculomegaly, cystic kidney disease | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set