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 |
3437059016 | Familial scaphocephaly syndrome McGillivray type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3437060014 | Familial scaphocephaly syndrome McGillivray type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3437061013 | Scaphocephaly, macrocephaly, maxillary retrusion, intellectual disability syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3437062018 | A rare craniosynostosis syndrome with characteristics of scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability. It has been reported in 11 patients from a three-generation family. The patients had variable dysmorphic features including high forehead, marked midface hypoplasia with severe maxillary retrusion, relative or absolute prognathism, and malocclusion. More severely affected patients were male and had intellectual disability. Molecular analysis revealed a K526E mutation of the fibroblast growth factor receptor 2 gene FGFR2. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3991131000052116 | familjär skafocefali av typen McGillivray | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial scaphocephaly syndrome McGillivray type (disorder) | Is a | skafocefali | false | Inferred relationship | Some | ||
Familial scaphocephaly syndrome McGillivray type (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Familial scaphocephaly syndrome McGillivray type (disorder) | Is a | Craniosynostosis syndrome | false | Inferred relationship | Some | ||
Familial scaphocephaly syndrome McGillivray type (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Familial scaphocephaly syndrome McGillivray type (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Familial scaphocephaly syndrome McGillivray type (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Associated morphology | medfödd onormal form | false | Inferred relationship | Some | 2 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Finding site | Bone structure of cranium | true | Inferred relationship | Some | 2 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Associated morphology | Congenital premature fusion | false | Inferred relationship | Some | 3 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Finding site | Structure of sagittal suture of skull | false | Inferred relationship | Some | 3 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Is a | Interparietal craniosynostosis (disorder) | true | Inferred relationship | Some | ||
Familial scaphocephaly syndrome McGillivray type (disorder) | Is a | Congenital abnormality of skull shape | true | Inferred relationship | Some | ||
Familial scaphocephaly syndrome McGillivray type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Finding site | Structure of sagittal suture of skull | true | Inferred relationship | Some | 1 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Associated morphology | Congenital premature fusion | true | Inferred relationship | Some | 1 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Associated morphology | Abnormal shape (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Familial scaphocephaly syndrome McGillivray type (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Familial scaphocephaly syndrome McGillivray type (disorder) | Is a | Congenital anomaly of bone and joint | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets