Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5068781011 | B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5068782016 | BILU (B-cell immunodeficiency, limb, urogenital) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5068783014 | B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5415038016 | BILU syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5415040014 | Agammaglobulinemia due to TOP2B mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5415041013 | Hoffman syndrome due to TOP2B deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5415042018 | Agammaglobulinaemia due to TOP2B mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5400139015 | A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by almost complete lack of B-cells and severe hypogammaglobulinemia, anomalies of the hands and feet, urogenital malformations, and characteristic facial dysmorphism (including microcephaly, highly arched eyebrows, hypoplastic alae nasi, and micrognathia). Most patients are developmentally normal, although moderate mental retardation has also been described. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400140018 | A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by almost complete lack of B-cells and severe hypogammaglobulinaemia, anomalies of the hands and feet, urogenital malformations, and characteristic facial dysmorphism (including microcephaly, highly arched eyebrows, hypoplastic alae nasi, and micrognathia). Most patients are developmentally normal, although moderate mental retardation has also been described. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Is a | Congenital agammaglobulinemia | true | Inferred relationship | Some | ||
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Is a | Multiple malformation syndrome with facial-limb defects as major feature | true | Inferred relationship | Some | ||
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Is a | Congenital abnormality of foot and toes (disorder) | true | Inferred relationship | Some | ||
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Is a | Genitourinary congenital anomalies | true | Inferred relationship | Some | ||
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Is a | Congenital anomaly of hand (disorder) | true | Inferred relationship | Some | ||
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Is a | Genetic disease | false | Inferred relationship | Some | ||
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Finding site | Structure of genitourinary system (body structure) | true | Inferred relationship | Some | 1 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Finding site | Foot structure | true | Inferred relationship | Some | 2 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Finding site | Hand structure | true | Inferred relationship | Some | 3 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 4 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 4 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 4 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 5 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 5 | |
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) | Is a | Hereditary disorder of immune system | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
Description inactivation indicator reference set