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 |
5401200010 | A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401201014 | A rare congenital limb malformation characterised by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
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 |
5476781000241114 | fémur bifide concomitant d'une ectrodactylie monodactyle | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3383871001000110 | Gollop-Wolfgang-Komplex | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Is a | Ectrodactyly | true | Inferred relationship | Some | ||
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Is a | Congenital anomaly of femur | false | Inferred relationship | Some | ||
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Is a | Connective tissue hereditary disorder | false | Inferred relationship | Some | ||
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Associated morphology | Congenital absence | false | Inferred relationship | Some | 2 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Finding site | Entire digit | true | Inferred relationship | Some | 2 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Associated morphology | Congenital notch | false | Inferred relationship | Some | 3 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Finding site | Bone structure of femur | false | Inferred relationship | Some | 3 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Associated morphology | Congenital notch | true | Inferred relationship | Some | 1 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Associated morphology | Absence (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Finding site | Structure of femur | false | Inferred relationship | Some | 1 | |
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Is a | Congenital abnormal shape of femur | true | Inferred relationship | Some | ||
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly. | Finding site | Bone structure of femur | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)