| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Congenital quadriplegia |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Paraplegic cerebral palsy (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Monoplegic cerebral palsy affecting upper limb (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Quadriplegic cerebral palsy (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Monoplegic cerebral palsy affecting lower limb |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Hemiplegic cerebral palsy |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Hypotonic cerebral palsy |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Double athetosis |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Cerebral palsy, not congenital or infantile, acute |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Dyskinetic cerebral palsy |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Monoplegic cerebral palsy (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| A form of spastic cerebral palsy affecting two limbs; usually the legs are affected more than the arms. |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Spastic cerebral palsy |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Spastic tetraplegia with rigidity syndrome (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| A form of dyskinetic cerebral palsy with slow, writhing movements that are often repetitive, sinuous, and rhythmic. |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Dystonic/rigid cerebral palsy |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Cerebral palsy |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| A less common type of cerebral palsy defined by decreased and/or fluctuating muscle tone; multiple forms of non-spastic cerebral palsy are each characterised by particular impairments; one of the main characteristics of non-spastic cerebral palsy is involuntary movement. Subtypes include ataxic and dyskinetic forms. |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| A form of dyskinetic cerebral palsy with involuntary movements accompanied by an abnormal, sustained posture. |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Choreic cerebral palsy (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| A form of dyskinetic cerebral palsy with a combination of chorea and athetosis; movements are irregular, but twisting and curving. |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Mixed cerebral palsy |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Bilateral cerebral palsy (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| A form of spastic cerebral palsy affecting three limbs; this could be both arms and a leg, or both legs and an arm. In some instances, it has referred to one upper and one lower extremity and the face. |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Pentaplegic cerebral palsy |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Worster-Drought syndrome (WDS) is a form of cerebral palsy characterised by congenital pseudobulbar (suprabulbar) paresis manifesting as selective weakness of the lips, tongue and soft palate, dysphagia, dysphonia, drooling and jaw jerking. |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Infantile-onset autosomal recessive non progressive cerebellar ataxia |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| An extremely rare multiple congenital anomalies/dysmorphic syndrome with characteristics of craniofacial dysmorphism including microbrachycephaly, sloping forehead, micro/anophthalmia, large ears, prominent nasal root, mild micrognathia and cleft palate. The syndrome is associated with cerebral palsy with choreoathetoid movements, intellectual disability, dextrocardia and longitudinal folding of plantae pedis. There have been no further descriptions in the literature since 1992. |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Congenital non-progressive ataxia |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Non-progressive hereditary glomerulonephritis (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| A rare autosomal recessive cerebellar ataxia characterized by early onset of non- or slowly progressive cerebellar signs and symptoms including truncal and gait ataxia, dysarthria, dysmetria, dysdiadochokinesis, tremor, and nystagmus. Delayed psychomotor development and intellectual disability are variable. Additional reported features are spasticity, hypotonia, cataracts, and sensorineural hearing loss, among others. Brain imaging shows cerebellar atrophy. |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| X-linked non progressive cerebellar ataxia (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Peripheral pterygium, stationary |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Stationary peripheral pterygium of right eye |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Stationary peripheral pterygium of left eye (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Stationary peripheral pterygium of bilateral eyes (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Congenital insensitivity to pain with severe intellectual disability (disorder) |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
| Dysequilibrium syndrome |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Non-progressive cerebellar ataxia |
Clinical course |
True |
Non-progressive (qualifier value) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
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