Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Contusion of cerebellum due to birth trauma (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Traumatic hemorrhage of cerebellum due to birth trauma (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Focal traumatic hemorrhage of cerebellum (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Focal non-hemorrhagic contusion of cerebellum (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Posterior inferior cerebellar artery syndrome |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebellar pressure cone (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Cerebellar laceration with concussion (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Boucher Neuhäuser syndrome |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Multiple focal injuries of cerebellum |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Traumatic haemorrhage of cerebellum |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Neonatal spontaneous cerebellar hemorrhage (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Focal laceration of cerebellum (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Primary glioblastoma multiforme of cerebellum (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Syndrome with characteristics of congenital cerebellar hypoplasia, endosteal sclerosis, hypotonia, ataxia, mild to moderate developmental delay, short stature, hip dislocation, and tooth eruption disturbances. It has been described in four patients. Less common manifestations are microcephaly, strabismus, nystagmus, optic atrophy and dysarthria. It is appears to be transmitted as an autosomal recessive trait. |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Thrombosis of left cerebellar artery (disorder) |
Finding site |
False |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Right cerebellar artery thrombosis |
Finding site |
False |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Autosomal dominant cerebellar ataxia type 2 |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebellum present (finding) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebellar infectious cyst |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Granuloma of cerebellum (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Combined oxidative phosphorylation defect type 29 (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
X-linked intellectual developmental disorder Christianson type (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Spinocerebellar ataxia due to vitamin E deficiency |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Tubulinopathy-associated dysgyria (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Severe oculo-renal-cerebellar syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Progressive cerebello-cerebral atrophy (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Spinocerebellar ataxia type 41 (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Spinocerebellar ataxia type 42 |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Spinocerebellar ataxia type 43 |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cerebellar ataxia with oculomotor apraxia type 4 |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Lethal brain and heart developmental defects syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Aprosencephaly cerebellar dysgenesis |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Cerebellar-facial-dental syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebellar function test (procedure) |
Procedure site - Indirect (attribute) |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Finger-to-finger test |
Procedure site - Indirect (attribute) |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Finger-to-nose test |
Procedure site - Indirect (attribute) |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Heel-to-knee test |
Procedure site - Indirect (attribute) |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Amyotrophic lateral sclerosis with cerebellar dysfunction |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Amyotrophic lateral sclerosis with spinocerebellar ataxia (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autoimmune cerebellar degeneration |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autoimmune inflammation of cerebellum (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary medulloblastoma of cerebellum (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary malignant glioma of cerebellum (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Clinically isolated syndrome of cerebellum (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fetal non-traumatic cerebellar hemorrhage |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Early neonatal non-traumatic cerebellar hemorrhage (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Drug-induced cerebellar ataxia |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cerebellar ataxia caused by chemical (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Spinocerebellar ataxia type 46 (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Spinocerebellar ataxia type 45 (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acquired cerebellar atrophy |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital pontocerebellar hypoplasia type 11 (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital pontocerebellar hypoplasia type 12 |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital pontocerebellar hypoplasia type 13 |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital pontocerebellar hypoplasia type 14 |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pumilio RNA binding family member 1-related cerebellar ataxia (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Dysequilibrium syndrome |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Nontraumatic edema of cerebellum (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebellar edema |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Edema of cerebellum due to trauma (disorder) |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Posterior cord syndrome due to Friedreich ataxia |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Cerebellar haemangioblastoma |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebellar ataxia with quadrupedal gait |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Non-progressive cerebellar ataxia |
Finding site |
True |
Cerebellar structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |