Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3304392013 | Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304393015 | Bifid femur co-occurrent with monodactylous ectrodactyly | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304394014 | Gollop Wolfgang complex | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3304396011 | Bifid femur with monodactylous ectrodactyly | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304395010 | A very rare malformation with main features of ectrodactyly of the hand and ipsilateral bifurcation of the femur. Approximately 200 cases have been reported worldwide. Congenital aplasia/hypoplasia of the tibia, accompanied by pre-axial oligodactyly or monodactyly of the feet, may also be present. In most cases, the bifurcation of the distal femur is unilateral. Patients are often small. Autosomal dominant and autosomal recessive modes of transmission have been suggested. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5453741000172115 | fémur bifide concomitant d'une ectrodactylie monodactyle | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
5453721000172112 | bifide femur gelijktijdig met 'monodactylous ectrodactyly' | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
5453731000172110 | Gollop-Wolfgangcomplex | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Is a | Ectrodactyly | true | Inferred relationship | Some | ||
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Is a | Congenital anomaly of femur (disorder) | false | Inferred relationship | Some | ||
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 2 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Finding site | Entire digit | true | Inferred relationship | Some | 2 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Associated morphology | Congenital notch | false | Inferred relationship | Some | 3 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Finding site | Bone structure of femur | false | Inferred relationship | Some | 3 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Associated morphology | Congenital notch | true | Inferred relationship | Some | 1 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Associated morphology | Absence (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Finding site | Structure of femur (body structure) | true | Inferred relationship | Some | 1 | |
Bifid femur co-occurrent with monodactylous ectrodactyly (disorder) | Is a | Congenital abnormal shape of femur | true | Inferred relationship | Some | ||
Bifid femur co-occurrent with monodactylous ectrodactyly (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