MCID: BSL005
MIFTS: 22

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 simultanagnosia and persistent fetal circulation syndrome. An important gene associated with Basal Ganglia Cerebrovascular Disease is SNRPD3 (Small Nuclear Ribonucleoprotein D3 Polypeptide), and among its related pathways/superpathways are Folate Metabolism and Cell adhesion_Plasmin signaling. Related phenotypes are liver/biliary system and renal/urinary system

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 47)
# Related Disease Score Top Affiliating Genes
1 simultanagnosia 10.1 CTBS APOE
2 persistent fetal circulation syndrome 10.0 POMC CTBS
3 alzheimer disease 17 9.9 PLAT APOE
4 hemorrhage, intracerebral 9.9 PLAT APOE
5 medulloadrenal hyperfunction 9.8 POMC PLG
6 spinal muscular atrophy 9.7 SNRPD3 SNRPD2 SNRPD1
7 ligneous conjunctivitis 9.7 PLG PLAT
8 anterior cerebral artery infarction 9.7 PLG PLAT
9 basilar artery occlusion 9.7 PLG PLAT
10 acute cor pulmonale 9.7 PLG PLAT
11 acute pulmonary heart disease 9.7 PLG PLAT
12 marantic endocarditis 9.7 PLG PLAT
13 thoracic outlet syndrome 9.7 PLG PLAT
14 vertebral artery occlusion 9.7 PLG PLAT
15 brain stem infarction 9.7 PLG PLAT
16 inferior myocardial infarction 9.7 PLG PLAT
17 cerebral falx meningioma 9.7 PLG PLAT
18 intracranial embolism 9.7 PLG PLAT
19 conversion disorder 9.7 PLG PLAT
20 hereditary angioedema with normal c1inh 9.7 PLG PLAT
21 posterior cerebral artery infarction 9.7 PLG PLAT
22 middle cerebral artery infarction 9.7 PLG PLAT
23 central retinal artery occlusion 9.7 PLG PLAT
24 cerebral artery occlusion 9.7 PLG APOE
25 occlusion precerebral artery 9.7 PLG PLAT
26 encephalopathy, familial, with neuroserpin inclusion bodies 9.7 PLG PLAT
27 post-thrombotic syndrome 9.6 PLG PLAT
28 obstructive hydrocephalus 9.6 PLG PLAT
29 cardiac tamponade 9.6 PLG PLAT
30 intracranial thrombosis 9.6 PLG PLAT
31 facial nerve disease 9.6 PLG PLAT
32 thrombophilia due to activated protein c resistance 9.6 PLG PLAT
33 carotid artery occlusion 9.6 PLG PLAT
34 thrombophlebitis 9.6 PLG PLAT
35 central retinal vein occlusion 9.6 PLG PLAT
36 coronary thrombosis 9.6 PLG PLAT
37 intermediate coronary syndrome 9.5 PLG PLAT
38 pulmonary artery disease 9.5 PLG PLAT
39 hepatic veno-occlusive disease 9.4 PLG PLAT
40 carotid artery disease 9.3 PLG PLAT APOE
41 aphasia 9.3 PLG PLAT APOE
42 vein disease 9.3 PLG PLAT
43 migraine with or without aura 1 9.2 POMC PLG APOE
44 speech and communication disorders 8.9 POMC PLG PLAT APOE
45 stroke, ischemic 8.8 PLG PLAT APOE
46 intracranial berry aneurysm 8.6 POMC PLG PLAT EXOSC10 APOE
47 hypertension, essential 8.5 POMC POLB PLG PLAT APOE

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

MGI Mouse Phenotypes related to Basal Ganglia Cerebrovascular Disease:

45
# Description MGI Source Accession Score Top Affiliating Genes
1 liver/biliary system MP:0005370 9.35 APOE CTBS PLG POLB POMC
2 renal/urinary system MP:0005367 9.02 APOE CTBS PLG POLB POMC

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

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

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

# Super pathways Score Top Affiliating Genes
1
Show member pathways
11.77 PLG PLAT APOE
2 11.06 PLG PLAT
3 11 PLG PLAT
4 10.52 PLG PLAT
5 10.52 SNRPD3 SNRPD2 SNRPD1
6 10.07 PLG PLAT

GO Terms for Basal Ganglia Cerebrovascular Disease

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

(show all 17)
# Name GO ID Score Top Affiliating Genes
1 spliceosomal complex GO:0005681 9.74 SNRPD3 SNRPD2 SNRPD1
2 catalytic step 2 spliceosome GO:0071013 9.73 SNRPD3 SNRPD2 SNRPD1
3 U2-type precatalytic spliceosome GO:0071005 9.7 SNRPD3 SNRPD2 SNRPD1
4 U4/U6 x U5 tri-snRNP complex GO:0046540 9.69 SNRPD3 SNRPD2 SNRPD1
5 U1 snRNP GO:0005685 9.67 SNRPD3 SNRPD2 SNRPD1
6 U2-type catalytic step 2 spliceosome GO:0071007 9.65 SNRPD3 SNRPD2 SNRPD1
7 U12-type spliceosomal complex GO:0005689 9.63 SNRPD3 SNRPD2 SNRPD1
8 U2 snRNP GO:0005686 9.61 SNRPD3 SNRPD2 SNRPD1
9 U5 snRNP GO:0005682 9.58 SNRPD3 SNRPD2 SNRPD1
10 spliceosomal tri-snRNP complex GO:0097526 9.55 SNRPD3 SNRPD1
11 commitment complex GO:0000243 9.54 SNRPD3 SNRPD1
12 precatalytic spliceosome GO:0071011 9.54 SNRPD3 SNRPD2 SNRPD1
13 SMN-Sm protein complex GO:0034719 9.5 SNRPD3 SNRPD2 SNRPD1
14 small nuclear ribonucleoprotein complex GO:0030532 9.43 SNRPD3 SNRPD2 SNRPD1
15 U4 snRNP GO:0005687 9.33 SNRPD3 SNRPD2 SNRPD1
16 methylosome GO:0034709 9.13 SNRPD3 SNRPD2 SNRPD1
17 pICln-Sm protein complex GO:0034715 8.8 SNRPD3 SNRPD2 SNRPD1

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

# Name GO ID Score Top Affiliating Genes
1 RNA splicing GO:0008380 9.58 SNRPD3 SNRPD2 SNRPD1
2 mRNA splicing, via spliceosome GO:0000398 9.54 SNRPD3 SNRPD2 SNRPD1
3 spliceosomal complex assembly GO:0000245 9.32 SNRPD2 SNRPD1
4 fibrinolysis GO:0042730 9.26 PLG PLAT
5 trans-synaptic signaling by BDNF, modulating synaptic transmission GO:0099183 9.16 PLG PLAT
6 spliceosomal snRNP assembly GO:0000387 9.13 SNRPD3 SNRPD2 SNRPD1
7 import into nucleus GO:0051170 8.8 SNRPD3 SNRPD2 SNRPD1

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

# Name GO ID Score Top Affiliating Genes
1 signaling receptor binding GO:0005102 9.26 POMC PLG PLAT APOE
2 telomerase RNA binding GO:0070034 9.16 SNRPD3 EXOSC10
3 U1 snRNP binding GO:1990446 8.62 SNRPD3 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
Content
Loading form....