Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3736387018 | Autosomal dominant aplasia and myelodysplasia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3736388011 | Autosomal dominant aplasia and myelodysplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3736389015 | Autosomal dominant aplastic anaemia and myelodysplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3736390012 | Autosomal dominant aplastic anemia and myelodysplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3736391011 | A rare genetic haematologic disorder characterised by bone marrow failure which manifests with aplastic anaemia and/or myelodysplasia, associated with hearing/ear abnormalities (such as deafness, labyrinthitis), inherited in an autosomal dominant manner. Caused by heterozygous mutation in the SRP72 gene on chromosome 4q12. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3736392016 | A rare genetic hematologic disorder characterized by bone marrow failure which manifests with aplastic anemia and/or myelodysplasia, associated with hearing/ear abnormalities (such as deafness, labyrinthitis), inherited in an autosomal dominant manner. Caused by heterozygous mutation in the SRP72 gene on chromosome 4q12. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant aplasia and myelodysplasia (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant aplasia and myelodysplasia (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Autosomal dominant aplasia and myelodysplasia (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Autosomal dominant aplasia and myelodysplasia (disorder) | Finding site | Bone marrow structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant aplasia and myelodysplasia (disorder) | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant aplasia and myelodysplasia (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Autosomal dominant aplasia and myelodysplasia (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal dominant aplasia and myelodysplasia (disorder) | Is a | Bone marrow disorder | true | Inferred relationship | Some | ||
Autosomal dominant aplasia and myelodysplasia (disorder) | Is a | Congenital deafness | true | Inferred relationship | Some | ||
Autosomal dominant aplasia and myelodysplasia (disorder) | Finding site | Inner ear structure (body structure) | true | Inferred relationship | Some | 2 | |
Autosomal dominant aplasia and myelodysplasia (disorder) | Is a | Congenital anomaly of ear with impairment of hearing | true | Inferred relationship | Some | ||
Autosomal dominant aplasia and myelodysplasia (disorder) | Is a | Congenital anomaly of inner ear | true | Inferred relationship | Some | ||
Autosomal dominant aplasia and myelodysplasia (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 3 | |
Autosomal dominant aplasia and myelodysplasia (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets