Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire cerebellar vermis |
Is a |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Superior vermis structure |
Is a |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Inferior vermis structure |
Is a |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Nodulus cerebelli |
Is a |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Paleocerebellar structure (body structure) |
Is a |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Structure of cerebellar declive (body structure) |
Is a |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Structure of lingula of cerebellum (body structure) |
Is a |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cerebellar folium vermis |
Is a |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cerebellar pyramis |
Is a |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cerebellar tuber |
Is a |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Aplasia of the vermis |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Familial aplasia of the vermis |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Gillespie syndrome |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Absence of the vermis |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dandy-Walker syndrome (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dandy-Walker syndrome with spina bifida |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Absence of the vermis |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dandy-Walker syndrome (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Absence of the vermis |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Aplasia of the vermis |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dandy-Walker syndrome with spina bifida |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Familial aplasia of the vermis |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Familial aplasia of the vermis |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Aplasia of the vermis |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Rhombencephalosynapsis (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Rhombencephalosynapsis (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dandy-Walker syndrome (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Dandy-Walker syndrome with spina bifida |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Familial aplasia of the vermis |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Aplasia of the vermis |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Rhombencephalosynapsis (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Joubert syndrome |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Joubert syndrome with ocular defect |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Joubert syndrome with renal defect |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A very rare genetic disorder characterized by the following congenital malformations: hydrocephalus (due to Dandy-Walker anomaly), cleft palate, and severe joint contractures. |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
9 |
A very rare genetic disorder characterized by the following congenital malformations: hydrocephalus (due to Dandy-Walker anomaly), cleft palate, and severe joint contractures. |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
14 |
Pettigrew syndrome |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Pettigrew syndrome |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
9 |
Joubert syndrome with congenital hepatic fibrosis (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Joubert syndrome with oculorenal defect (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Joubert syndrome with oculorenal defect (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Joubert syndrome with orofaciodigital defect |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
A rare, syndromic intellectual disability characterized by macrocephaly, short stature, intellectual disability, variable degree of spastic paraplegia, central nervous system malformations (hydrocephalus, Dandy-Walker malformation), and dysmorphic features, such as high and broad forehead, midface hypoplasia, and small and broad hands and feet. There have been no further descriptions in the literature since 1993. |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
9 |
A rare, syndromic intellectual disability characterized by macrocephaly, short stature, intellectual disability, variable degree of spastic paraplegia, central nervous system malformations (hydrocephalus, Dandy-Walker malformation), and dysmorphic features, such as high and broad forehead, midface hypoplasia, and small and broad hands and feet. There have been no further descriptions in the literature since 1993. |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
10 |
Gomez Lopez Hernandez syndrome (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Joubert syndrome with Jeune asphyxiating thoracic dystrophy (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Dandy-Walker malformation with postaxial polydactyly syndrome (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
A rare multiple congenital anomalies/dysmorphic syndrome characterised by severe intellectual deficit, Dandy-Walker malformation, macrocephaly, severe myopia, brachytelephalangy with short and broad fingernails, and dysmorphic facial features (such as thick eyebrows, synophrys, epicanthal folds, low-set ears, short philtrum, and high-arched palate). Additional reported manifestations include seizures and skeletal and genital anomalies, among others. There have been no further descriptions in the literature since 1989. |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
12 |
Dandy-Walker malformation with postaxial polydactyly syndrome (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
A rare multiple congenital anomalies/dysmorphic syndrome characterised by severe intellectual deficit, Dandy-Walker malformation, macrocephaly, severe myopia, brachytelephalangy with short and broad fingernails, and dysmorphic facial features (such as thick eyebrows, synophrys, epicanthal folds, low-set ears, short philtrum, and high-arched palate). Additional reported manifestations include seizures and skeletal and genital anomalies, among others. There have been no further descriptions in the literature since 1989. |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
9 |
Porencephaly, cerebellar hypoplasia, internal malformations syndrome (disorder) |
Finding site |
False |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Porencephaly, cerebellar hypoplasia, internal malformations syndrome (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Isolated hypoplasia of cerebellar vermis (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
X-linked cerebral, cerebellar, coloboma syndrome (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A very rare genetic disorder characterized by the following congenital malformations: hydrocephalus (due to Dandy-Walker anomaly), cleft palate, and severe joint contractures. |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Joubert syndrome with ocular defect |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pettigrew syndrome |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Joubert syndrome with congenital hepatic fibrosis (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
A rare multiple congenital anomalies/dysmorphic syndrome characterised by severe intellectual deficit, Dandy-Walker malformation, macrocephaly, severe myopia, brachytelephalangy with short and broad fingernails, and dysmorphic facial features (such as thick eyebrows, synophrys, epicanthal folds, low-set ears, short philtrum, and high-arched palate). Additional reported manifestations include seizures and skeletal and genital anomalies, among others. There have been no further descriptions in the literature since 1989. |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Joubert syndrome with Jeune asphyxiating thoracic dystrophy (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare, syndromic intellectual disability characterized by macrocephaly, short stature, intellectual disability, variable degree of spastic paraplegia, central nervous system malformations (hydrocephalus, Dandy-Walker malformation), and dysmorphic features, such as high and broad forehead, midface hypoplasia, and small and broad hands and feet. There have been no further descriptions in the literature since 1993. |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Dandy-Walker malformation with postaxial polydactyly syndrome (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Joubert syndrome with renal defect |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Joubert syndrome with orofaciodigital defect |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Gomez Lopez Hernandez syndrome (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A very rare genetic disorder characterized by the following congenital malformations: hydrocephalus (due to Dandy-Walker anomaly), cleft palate, and severe joint contractures. |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
A rare multiple congenital anomalies/dysmorphic syndrome characterised by severe intellectual deficit, Dandy-Walker malformation, macrocephaly, severe myopia, brachytelephalangy with short and broad fingernails, and dysmorphic facial features (such as thick eyebrows, synophrys, epicanthal folds, low-set ears, short philtrum, and high-arched palate). Additional reported manifestations include seizures and skeletal and genital anomalies, among others. There have been no further descriptions in the literature since 1989. |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Dandy-Walker malformation with postaxial polydactyly syndrome (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pettigrew syndrome |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A rare, syndromic intellectual disability characterized by macrocephaly, short stature, intellectual disability, variable degree of spastic paraplegia, central nervous system malformations (hydrocephalus, Dandy-Walker malformation), and dysmorphic features, such as high and broad forehead, midface hypoplasia, and small and broad hands and feet. There have been no further descriptions in the literature since 1993. |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome (disorder) |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Isolated agenesis of cerebellar vermis |
Finding site |
True |
Cerebellar vermis structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |