MCID: BSL005
MIFTS: 21

Basal Ganglia Cerebrovascular Disease

Categories: Cardiovascular diseases, Neuronal diseases

Aliases & Classifications for Basal Ganglia Cerebrovascular Disease

MalaCards integrated aliases for Basal Ganglia Cerebrovascular Disease:

Name: Basal Ganglia Cerebrovascular Disease 12 43 15 17 71

Classifications:



External Ids:

Disease Ontology 12 DOID:10991
MeSH 43 D020144
UMLS 71 C0751739

Summaries for Basal Ganglia Cerebrovascular Disease

MalaCards based summary : Basal Ganglia Cerebrovascular Disease is related to aphasia and scalp dermatosis. An important gene associated with Basal Ganglia Cerebrovascular Disease is SNRPD2 (Small Nuclear Ribonucleoprotein D2 Polypeptide), and among its related pathways/superpathways are Complement and coagulation cascades and Microglia Activation During Neuroinflammation: Overview. Affiliated tissues include heart and brain.

Related Diseases for Basal Ganglia Cerebrovascular Disease

Diseases related to Basal Ganglia Cerebrovascular Disease via text searches within MalaCards or GeneCards Suite gene sharing:

(show all 42)
# Related Disease Score Top Affiliating Genes
1 aphasia 29.5 PLG PLAT
2 scalp dermatosis 10.0 SNRPD2 SNRPD1
3 anterior cerebral artery infarction 9.8 PLG PLAT
4 ligneous conjunctivitis 9.8 PLG PLAT
5 basilar artery occlusion 9.8 PLG PLAT
6 acute cor pulmonale 9.8 PLG PLAT
7 acute pulmonary heart disease 9.8 PLG PLAT
8 marantic endocarditis 9.8 PLG PLAT
9 brain stem infarction 9.8 PLG PLAT
10 thoracic outlet syndrome 9.8 PLG PLAT
11 inferior myocardial infarction 9.8 PLG PLAT
12 conversion disorder 9.8 PLG PLAT
13 intracranial embolism 9.8 PLG PLAT
14 basilar artery insufficiency 9.8 PLG PLAT
15 vitreous detachment 9.8 PLG PLAT
16 central retinal artery occlusion 9.8 PLG PLAT
17 middle cerebral artery infarction 9.8 PLG PLAT
18 carotid artery thrombosis 9.8 PLG PLAT
19 occlusion precerebral artery 9.8 PLG PLAT
20 obstructive hydrocephalus 9.7 PLG PLAT
21 encephalopathy, familial, with neuroserpin inclusion bodies 9.7 PLG PLAT
22 post-thrombotic syndrome 9.7 PLG PLAT
23 intracranial thrombosis 9.7 PLG PLAT
24 thrombophilia due to activated protein c resistance 9.7 PLG PLAT
25 thrombophilia 9.7 PLG PLAT
26 carotid artery occlusion 9.7 PLG PLAT
27 thrombophlebitis 9.7 PLG PLAT
28 central retinal vein occlusion 9.7 PLG PLAT
29 coronary thrombosis 9.7 PLG PLAT
30 intermediate coronary syndrome 9.7 PLG PLAT
31 pulmonary artery disease 9.7 PLG PLAT
32 cerebral arterial disease 9.7 PLG PLAT
33 hepatic veno-occlusive disease 9.7 PLG PLAT
34 vein disease 9.7 PLG PLAT
35 carotid artery disease 9.6 PLG PLAT
36 heart conduction disease 9.6 PLG PLAT
37 afibrinogenemia, congenital 9.6 PLG PLAT
38 disseminated intravascular coagulation 9.6 PLG PLAT
39 intracranial berry aneurysm 9.5 PLG PLAT
40 atrial heart septal defect 9.5 PLG PLAT
41 patent foramen ovale 9.4 PLG PLAT
42 speech and communication disorders 9.2 PLG PLAT

Graphical network of the top 20 diseases related to Basal Ganglia Cerebrovascular Disease:



Diseases related to Basal Ganglia Cerebrovascular Disease

Symptoms & Phenotypes for Basal Ganglia Cerebrovascular Disease

Drugs & Therapeutics for Basal Ganglia Cerebrovascular Disease

Search Clinical Trials , NIH Clinical Center for Basal Ganglia Cerebrovascular Disease

Cochrane evidence based reviews: basal ganglia cerebrovascular disease

Genetic Tests for Basal Ganglia Cerebrovascular Disease

Anatomical Context for Basal Ganglia Cerebrovascular Disease

MalaCards organs/tissues related to Basal Ganglia Cerebrovascular Disease:

40
Heart, Brain

Publications for Basal Ganglia Cerebrovascular Disease

Variations for Basal Ganglia Cerebrovascular Disease

Expression for Basal Ganglia Cerebrovascular Disease

Search GEO for disease gene expression data for Basal Ganglia Cerebrovascular Disease.

Pathways for Basal Ganglia Cerebrovascular Disease

GO Terms for Basal Ganglia Cerebrovascular Disease

Cellular components related to Basal Ganglia Cerebrovascular Disease according to GeneCards Suite gene sharing:

(show all 14)
# Name GO ID Score Top Affiliating Genes
1 Schaffer collateral - CA1 synapse GO:0098685 9.54 PLG PLAT
2 catalytic step 2 spliceosome GO:0071013 9.52 SNRPD2 SNRPD1
3 U2-type precatalytic spliceosome GO:0071005 9.51 SNRPD2 SNRPD1
4 U4/U6 x U5 tri-snRNP complex GO:0046540 9.49 SNRPD2 SNRPD1
5 U2-type catalytic step 2 spliceosome GO:0071007 9.48 SNRPD2 SNRPD1
6 U12-type spliceosomal complex GO:0005689 9.46 SNRPD2 SNRPD1
7 U2 snRNP GO:0005686 9.43 SNRPD2 SNRPD1
8 U1 snRNP GO:0005685 9.4 SNRPD2 SNRPD1
9 SMN-Sm protein complex GO:0034719 9.37 SNRPD2 SNRPD1
10 U5 snRNP GO:0005682 9.32 SNRPD2 SNRPD1
11 small nuclear ribonucleoprotein complex GO:0030532 9.26 SNRPD2 SNRPD1
12 methylosome GO:0034709 9.16 SNRPD2 SNRPD1
13 U4 snRNP GO:0005687 8.96 SNRPD2 SNRPD1
14 pICln-Sm protein complex GO:0034715 8.62 SNRPD2 SNRPD1

Biological processes related to Basal Ganglia Cerebrovascular Disease according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 spliceosomal snRNP assembly GO:0000387 9.32 SNRPD2 SNRPD1
2 spliceosomal complex assembly GO:0000245 9.26 SNRPD2 SNRPD1
3 import into nucleus GO:0051170 9.16 SNRPD2 SNRPD1
4 fibrinolysis GO:0042730 8.96 PLG PLAT
5 trans-synaptic signaling by BDNF, modulating synaptic transmission GO:0099183 8.62 PLG PLAT

Molecular functions related to Basal Ganglia Cerebrovascular Disease according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 serine-type peptidase activity GO:0008236 8.96 PLG PLAT
2 U1 snRNP binding GO:1990446 8.62 SNRPD2 SNRPD1

Sources for Basal Ganglia Cerebrovascular Disease

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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