Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3008869012 | Manitoba oculotrichoanal syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3008917018 | MOTA - Manitoba oculotrichoanal syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3009421010 | Marles-Greenburg-Persaud syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3009686012 | Manitoba oculotrichoanal syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| 3009696015 | Marles syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Manitoba oculotrichoanal syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Manitoba oculotrichoanal syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
| Manitoba oculotrichoanal syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Manitoba oculotrichoanal syndrome | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
| Manitoba oculotrichoanal syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Manitoba oculotrichoanal syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Manitoba oculotrichoanal syndrome | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR