Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Is a | Disorder of brain (disorder) | true | Inferred relationship | Some | ||
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Finding site | Brain structure | false | Inferred relationship | Some | ||
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Is a | Paralytic syndrome | true | Inferred relationship | Some | ||
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Finding site | The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. | false | Inferred relationship | Some | 2 | |
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Clinical course | Non-progressive | true | Inferred relationship | Some | 1 | |
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Interprets | mouvement | false | Inferred relationship | Some | 4 | |
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Interprets | Movement observable | true | Inferred relationship | Some | 3 | |
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Has interpretation | Absent | true | Inferred relationship | Some | 3 | |
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Finding site | Brain structure | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A form of non-spastic cerebral palsy with decreased muscle tone, noticeably floppy muscles with poor or no head control. | Is a | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
A type of cerebral palsy defined by increased tone and pathological reflexes resulting in an abnormal pattern of movement and posture. | Is a | True | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
Congenital non-progressive ataxia | Is a | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
A form of athetoid cerebral palsy with bilateral involuntary movements. | Is a | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
A form of spastic cerebral palsy affecting the arm and/or leg on one side of the body. An ipsilateral upper and/or lower extremity is affected. | Is a | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
Infantile cerebral palsy | Is a | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
infirmité motrice cérébrale congénitale | Is a | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
Cerebral palsy, not congenital or infantile, acute | Is a | True | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
Other congenital cerebral palsy | Is a | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
Other infantile cerebral palsy NOS | Is a | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
Congenital cerebral palsy NOS | Is a | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
A form of spastic cerebral palsy affecting the lower half of the body, including both legs. | Is a | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
Family history: Cerebral palsy | Associated finding | False | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | 2 |
A less common type of cerebral palsy defined by decreased and/or fluctuating muscle tone; multiple forms of non-spastic cerebral palsy are each characterized by particular impairments; one of the main characteristics of non-spastic cerebral palsy is involuntary movement. Subtypes include ataxic and dyskinetic forms. | Is a | True | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
A form of cerebral palsy where no predominant motion can be determined; when it is a mixed CP form, i.e. spasticity with ataxia and/or dyskinesia, the child should be classified according to the dominant clinical feature | Is a | True | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
Worster-Drought syndrome (WDS) is a form of cerebral palsy characterized by congenital pseudobulbar (suprabulbar) paresis manifesting as selective weakness of the lips, tongue and soft palate, dysphagia, dysphonia, drooling and jaw jerking. | Is a | True | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | |
Neuromuscular scoliosis co-occurrent and due to cerebral palsy (disorder) | Due to | True | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | 1 |
Family history: Cerebral palsy | Associated finding | True | A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. | Inferred relationship | Some | 1 |
This concept is not in any reference sets