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.

autosomal recessive spinocerebellar ataxia 2

ID: DOID:0080061

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

Label: autosomal recessive spinocerebellar ataxia 2

Synonyms: autosomal recessive spinocerebellar ataxia 2

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

autosomal recessive spinocerebellar ataxia 2

DOID:0080061
autosomal recessive spinocerebellar ataxia 13

DOID:0080062
autosomal recessive spinocerebellar ataxia 11

DOID:0080063
autosomal recessive spinocerebellar ataxia 14

DOID:0080058
autosomal recessive spinocerebellar ataxia 20

DOID:0080066
autosomal recessive spinocerebellar ataxia 15

DOID:0080057
autosomal recessive spinocerebellar ataxia 17

DOID:0080064
autosomal recessive cerebellar ataxia

DOID:0050950
autosomal recessive spinocerebellar ataxia 12

DOID:0080060
autosomal recessive spinocerebellar ataxia 7

DOID:0080059
ataxia with oculomotor apraxia type 3

DOID:0060557
fragile X-associated tremor/ataxia syndrome

DOID:0050879
autosomal recessive spinocerebellar ataxia 10

DOID:0050999
X-linked hereditary ataxia

DOID:0050953
autosomal recessive spinocerebellar ataxia 19

DOID:0080065
spastic ataxia

DOID:0050952
hereditary ataxia

DOID:0050951
cerebellar ataxia

DOID:0050997
autosomal recessive spinocerebellar ataxia 16

DOID:0080029
Progressive cerebellar ataxia

HP:0002073
Dysarthria

HP:0001260
Charlevoix-Saguenay spastic ataxia

DOID:0050946
Alexia

HP:0010523
Loss of speech

HP:0002371
autosomal recessive spinocerebellar ataxia 18

DOID:0080042
D-xylose-importing ATPase activity

GO:0015614
Dysphonia

HP:0001618
ataxia with oculomotor apraxia type 2

DOID:0050755
recruitment of 3'\''-end processing factors to RNA polymerase II holoenzyme complex

GO:0034402
Aphasia

HP:0002381
Abnormality of the epiphyses of the middle phalanges of the hand

HP:0010244
spinocerebellar ataxia type 5

DOID:0050882
Pseudobulbar paralysis

HP:0007024
Abnormality of the proximal phalanx of the 4th finger

HP:0009284
Irregular epiphyses of the middle phalanges of the hand

HP:0010262
Neurological speech impairment

HP:0002167
Olivopontocerebellar atrophy

HP:0002542
Abnormality of the epiphysis of the distal phalanx of the 5th finger

HP:0009198
Triangular epiphyses of the middle phalanges of the hand

HP:0010267
neuromast regeneration

GO:0070657
Small epiphyses of the middle phalanges of the hand

HP:0010265
Asynergia

HP:0010869
Bracket epiphyses of the proximal phalanges of the hand

HP:0010269
protein localization to cell tip

GO:1990151
Dysgraphia

HP:0010526
Pseudoepiphyses of the middle phalanges of the hand

HP:0010264
Fragmentation of the epiphyses of the proximal phalanges of the hand

HP:0010272
Abnormality of the dentate nucleus

HP:0100321
lumbosacral plexus lesion

DOID:13913
Spastic ataxia

HP:0002497
infantile cerebellar-retinal degeneration

DOID:0050883
Enlarged epiphysis of the middle phalanx of the 4th finger

HP:0009217
Late-onset spinocerebellar degeneration

HP:0006904
Irregular epiphyses of the 4th finger

HP:0009398
protein localization to kinetochore

GO:0034501
mitochondrial complex III deficiency nuclear type 2

DOID:0060351
phragmoplast assembly

GO:0000914
protein localization to old growing cell tip

GO:1903858
Abnormality of hindbrain morphology

HP:0011282
Abnormality of the spinocerebellar tracts

HP:0003133
protein localization to kinetochore involved in kinetochore assembly

GO:1903394
Death in childhood

HP:0003819
Fragmentation of the epiphyses of the middle phalanges of the hand

HP:0010261
Total anomalous pulmonary venous return

HP:0005160
CHEMBL2204335

http://aber-owl.net/drug/CID011393561
protein localization to condensed chromosome

GO:1903083
Abnormality of the metencephalon

HP:0011283
Dysphasia

HP:0002357
Spoken Word Recognition Deficit

HP:0030391
sensory perception of salty taste

GO:0050914
spastic ataxia 7

DOID:0050945
benign pericardial teratoma

DOID:8012
protein localization to endosome

GO:0036010
Absent epiphysis of the distal phalanx of the 5th finger

HP:0003696
Triangular shaped middle phalanx of the 4th finger

HP:0009309
Stillbirth

HP:0003826
deep leiomyoma

DOID:5128
Gait apraxia

HP:0010521
Abnormality of the epiphysis of the middle phalanx of the 3rd finger

HP:0009334
Anarthria

HP:0002425
protein localization to vacuolar membrane

GO:1903778
secondary cell wall cellulose synthase complex

GO:0044568
tumor of the thecoma fibroma group

DOID:5472
pericardium leiomyoma

DOID:5137
Distal sensory impairment

HP:0002936
Enlarged epiphyses of the middle phalanges of the hand

HP:0010260
obsolete class II major histocompatibility complex antigen

GO:0003821
obsolete perillyl-CoA synthetase activity

GO:0018853
negative regulation of immunoglobulin mediated immune response

GO:0002890
Absent epiphyses of the proximal phalanges of the hand

HP:0010268
amyotrophic lateral sclerosis type 1

DOID:0060193
Atrophy of the dentate nucleus

HP:0007047
Fragmentation of the epiphysis of the proximal phalanx of the 2nd finger

HP:0009528
protein localization to cell leading edge

GO:1902463
spinocerebellar ataxia type 31

DOID:0050980
glucose:sodium symporter activity

GO:0005412
Fragmentation of the epiphyses of the phalanges of the hand

HP:0010232
no_name

GO:0061490
Fragmentation of the epiphyses of the 5th finger

HP:0009386
Irregular epiphysis of the distal phalanx of the 5th finger

HP:0009167

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