Bio2Vec

BIO-KNOWLEDGE-GRAPH

A knowledge graph of biological entities such as genes, gene functions, diseases, phenotypes and chemicals. Embeddings are generated with Walking RDF and OWL method.

spinocerebellar ataxia type 8

ID: DOID:0050959

Type: http://bio2vec.net/ontology/disease

Label: spinocerebellar ataxia type 8

Synonyms: spinocerebellar ataxia type 8

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

spinocerebellar ataxia type 8

DOID:0050959
spinocerebellar ataxia type 7

DOID:0050958
spinocerebellar ataxia type 6

DOID:0050956
spinocerebellar ataxia type 23

DOID:0050973
spinocerebellar ataxia type 16

DOID:0050966
spinocerebellar ataxia type 1

DOID:0050954
spinocerebellar ataxia type 13

DOID:0050963
spinocerebellar ataxia type 2

DOID:0050955
GRID2-related spinocerebellar ataxia

DOID:0050988
spinocerebellar ataxia type 28

DOID:0050977
spinocerebellar ataxia type 31

DOID:0050980
spinocerebellar ataxia type 29

DOID:0050978
hypomyelinating leukoencephalopathy

DOID:0050987
spinocerebellar ataxia type 17

DOID:0050967
spinocerebellar ataxia type 35

DOID:0050982
spinocerebellar ataxia type 18

DOID:0050969
spinocerebellar ataxia type 10

DOID:0050960
spinocerebellar ataxia type 15

DOID:0050965
spinocerebellar ataxia type 12

DOID:0050962
autosomal dominant cerebellar ataxia

DOID:0050968
spinocerebellar ataxia type 34

DOID:0050981
spinocerebellar ataxia type 20

DOID:0050971
spinocerebellar ataxia type 14

DOID:0050964
spinocerebellar ataxia type 5

DOID:0050882
spinocerebellar ataxia type 11

DOID:0050961
PRY

http://www.ncbi.nlm.nih.gov/gene/9081
spinocerebellar ataxia type 26

DOID:0050975
spinocerebellar ataxia type 36

DOID:0050983
spinocerebellar ataxia type 19/22

DOID:0050970
spinocerebellar ataxia type 40

DOID:0050986
spinocerebellar ataxia type 30

DOID:0050979
autosomal dominant type IV Ehlers-Danlos syndrome

DOID:14756
Decreased adiponectin level

HP:0030685
CHEBI:286544

http://aber-owl.net/drug/CID044341509
hereditary ataxia

DOID:0050951
TTTY2

http://www.ncbi.nlm.nih.gov/gene/60439
SLEB3

http://www.ncbi.nlm.nih.gov/gene/64695
spinocerebellar ataxia type 38

DOID:0050985
CHDM

http://www.ncbi.nlm.nih.gov/gene/121775
Pretesticular azoospermia

HP:0011963
MIR610

http://www.ncbi.nlm.nih.gov/gene/693195
spinocerebellar ataxia type 27

DOID:0050976
CCDC27

http://www.ncbi.nlm.nih.gov/gene/148870
no_name

DOID:13830
positive regulation of protein export from nucleus during meiotic anaphase II

GO:1900199
calcium ion transport from cytosol to endoplasmic reticulum

GO:1903515
formation of quadruple SL/U4/U5/U6 snRNP

GO:0000353
CHEMBL44665

http://aber-owl.net/drug/CID144290763
no_name

DOID:444
FUNDC2

http://www.ncbi.nlm.nih.gov/gene/65991
childhood malignant schwannoma

DOID:7732
spinocerebellar ataxia type 25

DOID:0050974
regulation of ribosomal large subunit export from nucleus

GO:2000203
Elevated diastolic blood pressure

HP:0005117
no_name

DOID:443
agraphia

DOID:0060223
GGTA1P

http://www.ncbi.nlm.nih.gov/gene/2681
X-linked hereditary ataxia

DOID:0050953
hypoglossal nerve disease

DOID:13814
no_name

GO:0006395
glicentin

http://aber-owl.net/drug/CID000126332
Asymmetrical distribution of flash visual evoked potentials

HP:0030463
spinocerebellar ataxia type 4

DOID:0050957
childhood brain stem glioma

DOID:6383
HSFY2

http://www.ncbi.nlm.nih.gov/gene/159119
Jerky ocular pursuit movements

HP:0008003
Abnormal adiponectin level

HP:0030684
Decreased number of large peripheral myelinated nerve fibers

HP:0003387
FRA11A

http://www.ncbi.nlm.nih.gov/gene/2438
positive regulation of the force of heart contraction involved in baroreceptor response to decreased systemic arterial blood pressure

GO:0001989
AC1NRXDU

http://aber-owl.net/drug/CID005274948
ST8

http://www.ncbi.nlm.nih.gov/gene/6765
CHEBI:399632

http://aber-owl.net/drug/CID144388668
childhood onset epileptic encephalopathy

DOID:0060475
SLITRK2

http://www.ncbi.nlm.nih.gov/gene/84631
no_name

DOID:14696
CHEBI:803492

http://aber-owl.net/drug/CID052941276
positive regulation of ribosomal subunit export from nucleus

GO:2000202
Progressive night blindness

HP:0007675
CHEBI:745225

http://aber-owl.net/drug/CID146906558
2-3 toe cutaneous syndactyly

HP:0005709
spinocerebellar ataxia type 37

DOID:0050984
positive regulation of lateral pseudopodium assembly

GO:0031277
Abnormality of the pons

HP:0007361
CHEBI:248566

http://aber-owl.net/drug/CID044324728
CHEMBL96334

http://aber-owl.net/drug/CID044326752
obsolete transportin

GO:0005649
Hypoplasia of the pons

HP:0012110
no_name

DOID:11655
LINC01387

http://www.ncbi.nlm.nih.gov/gene/100130480
Onion bulb formation

HP:0003383
LINC00574

http://www.ncbi.nlm.nih.gov/gene/80069
DUX5

http://www.ncbi.nlm.nih.gov/gene/26581
SCA9

http://www.ncbi.nlm.nih.gov/gene/140451
OR14J1

http://www.ncbi.nlm.nih.gov/gene/442191
no_name

DOID:2478
CHEBI:617969

http://aber-owl.net/drug/CID125258364
no_name

DOID:11053
no_name

DOID:10276
obsolete prolyl oligopeptidase activity

GO:0004287

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