Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
99071013 | Pelizaeus-Merzbacher disease, connatal variant | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
798500019 | Pelizaeus-Merzbacher disease, connatal variant (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
1231984012 | Type II congenital Pelizaeus-Merzbacher disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2672821000005113 | Pelizaeus-Merzbachers sygdom, konnatal variant | da | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | dansk modul |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Is a | Pelizaeus-Merzbacher disease (disorder) | true | Inferred relationship | Some | ||
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Associated morphology | Sudanophilic stain reaction | false | Inferred relationship | Some | 3 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Finding site | Structure of nervous system (body structure) | false | Inferred relationship | Some | 1 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 1 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Associated morphology | Myelin sheath alteration | false | Inferred relationship | Some | 1 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Associated morphology | Myelin sheath alteration | true | Inferred relationship | Some | 1 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 1 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Finding site | Structure of nervous system (body structure) | false | Inferred relationship | Some | 1 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 2 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Finding site | Myelinated nerve fiber structure | true | Inferred relationship | Some | 1 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Finding site | White matter structure of brain and spinal cord (body structure) | true | Inferred relationship | Some | 2 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Is a | Congenital degeneration of nervous system | true | Inferred relationship | Some | ||
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Is a | Congenital anomaly of central nervous system | true | Inferred relationship | Some | ||
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Pelizaeus-Merzbacher disease, connatal variant (disorder) | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets