Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3321293013 | Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3321294019 | Brachytelephalangy, facial dysmorphism, Kallmann syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3321295018 | A developmental anomaly with characteristics of brachytelephalangy, distinct craniofacial features (prominent square forehead, telecanthus, small nose, malar hypoplasia, smooth philtrum and thin upper lip), and relative to other family members, a short stature. These features may be associated with anosmia and hypogonadotropic hypogonadism (considered as Kallman syndrome). This anomaly has been described in a mother and her son and there have been no further descriptions in the literature since 1986. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 2 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Is a | Multiple malformation syndrome with facial-limb defects as major feature | true | Inferred relationship | Some | ||
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Is a | Short stature disorder | true | Inferred relationship | Some | ||
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Is a | Congenital anomaly of digit (disorder) | true | Inferred relationship | Some | ||
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Finding site | Digit structure | false | Inferred relationship | Some | 2 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 3 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Finding site | Face structure | false | Inferred relationship | Some | 3 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Finding site | Digit structure | true | Inferred relationship | Some | 1 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) | Interprets | Height / growth measure | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set