Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3451940015 | Familial isolated congenital asplenia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3451941016 | Familial isolated congenital asplenia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3451942011 | A rare non-syndromic potentially life-threatening visceral malformation with the absence of normal spleen function, resulting in a primary immunodeficiency. Typically, the condition manifests with severe, recurrent, overwhelming infections (especially pneumococcal sepsis) in otherwise apparently healthy infants. In adults with no history of severe sepsis in infancy, thrombocytosis may be the presenting sign. Howell-Jolly bodies on blood smears and an absent spleen on abdominal ultrasound examination are highly suggestive associated findings. There is evidence this disorder is caused by heterozygous mutation in the RPSA gene on chromosome 3p21. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial isolated congenital asplenia (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Familial isolated congenital asplenia (disorder) | Is a | Congenital absence of spleen | true | Inferred relationship | Some | ||
Familial isolated congenital asplenia (disorder) | Is a | Familial disease | true | Inferred relationship | Some | ||
Familial isolated congenital asplenia (disorder) | Is a | Hereditary disorder by system | true | Inferred relationship | Some | ||
Familial isolated congenital asplenia (disorder) | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
Familial isolated congenital asplenia (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Familial isolated congenital asplenia (disorder) | Finding site | Splenic structure | true | Inferred relationship | Some | 1 | |
Familial isolated congenital asplenia (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Familial isolated congenital asplenia (disorder) | Is a | Asplenia (disorder) | false | Inferred relationship | Some | ||
Familial isolated congenital asplenia (disorder) | Is a | Aplasia of spleen (disorder) | false | Inferred relationship | Some | ||
Familial isolated congenital asplenia (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Familial isolated congenital asplenia (disorder) | Associated morphology | Absence (morphologic abnormality) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets