Aliases & Classifications for Cerebritis

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Aliases & Descriptions for Cerebritis:

Name: Cerebritis 10 12 65

Classifications:



External Ids:

Disease Ontology10 DOID:3431
NCIt42 C27199
UMLS65 C0742115

Summaries for Cerebritis

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Wikipedia:68 Cerebritis is an infection of the brain that normally leads to the formation of an abscess within the... more...

MalaCards based summary: Cerebritis is related to cerebral sarcoidosis and hemoglobinuria. An important gene associated with Cerebritis is IRAK4 (Interleukin 1 Receptor Associated Kinase 4), and among its related pathways are 14-3-3 and Regulation of BAD Activity and Pertussis. Affiliated tissues include breast, lung and brain, and related mouse phenotypes are digestive/alimentary and hematopoietic system.

Related Diseases for Cerebritis

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Diseases related to Cerebritis via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50)    (show all 3016)
idRelated DiseaseScoreTop Affiliating Genes
1cerebral sarcoidosis33.6TNF, TNFRSF1B
2hemoglobinuria30.1SETD1A, SETD2
3venous insufficiency30.0AQP4, SETD2
4felty's syndrome29.9GRIK1, GRIK2
5bronchitis29.8GFAP, MAP2
6telangiectasis29.7TNF, TNFRSF1B
7brain stem glioma29.6TNF, TNFRSF1B
8inclusion body myositis29.6PRTN3, TNFRSF1B
9rheumatoid arthritis29.3CXCL1, CXCL5, PRTN3, TNF, TNFRSF1B
10spinal muscular atrophy29.0AQP4, CASP3, GFAP, TNF
11chronic cholangitis29.0AQP4, GFAP, TNF
12mucinous cystadenocarcinoma28.9CASP3, GRIK1, GRIK2, MAP2
13cerebral amyloid angiopathy12.7
14cerebral palsy12.6
15transient cerebral ischemia12.5
16cerebral palsy, ataxic, autosomal recessive12.5
17cerebral atherosclerosis12.5
18cerebral cavernous malformations-112.4
19cerebral ventricle cancer12.4
20cerebral amyloid angiopathy, dutch, italian, iowa, flemish, arctic variants12.4
21dyskinetic cerebral palsy12.4
22vasculopathy, retinal, with cerebral leukodystrophy12.4
23cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome12.4
24cerebral cavernous malformation, familial12.4
25cerebral aneurysms12.4
26spastic diplegia cerebral palsy12.3
27cerebral folate deficiency12.3
28spastic cerebral palsy12.3
29reversible cerebral vasoconstriction syndrome12.3
30cerebral palsy, spastic quadriplegic, 112.3
31cerebral hypoxia12.3
32cerebral cavernous malformations 312.3
33cerebral cavernous malformations-212.3
34hereditary cerebral amyloid angiopathy12.3
35cerebral atrophy12.3
36cerebral arteriosclerosis12.3
37cerebral hemorrhage12.3
38hypomyelination, global cerebral12.3
39middle cerebral artery infarction12.3
40cerebral palsy, spastic quadriplegic, 212.3
41microcephaly, progressive, seizures, and cerebral and cerebellar atrophy12.3
42cerebral creatine deficiency syndrome 312.3
43cerebral arteriopathy with subcortical infarcts and leukoencephalopathy12.3
44deafness, dystonia, and cerebral hypomyelination12.3
45neurodegeneration due to cerebral folate transport deficiency12.2
46cerebral meningioma12.2
47cerebral arteritis12.2
48cerebral creatine deficiency syndrome 212.2
49cerebral creatine deficiency syndrome 112.2
50mixed cerebral palsy12.2

Graphical network of the top 20 diseases related to Cerebritis:



Diseases related to cerebritis

Symptoms for Cerebritis

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Drugs & Therapeutics for Cerebritis

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Drugs for Cerebritis (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

idNameStatusPhaseClinical TrialsCas NumberPubChem Id
1Tissue Plasminogen ActivatorPhase 2202
2PlasminogenPhase 2198
3Fibrinolytic AgentsPhase 21567

Interventional clinical trials:

idNameStatusNCT IDPhase
1Minimally Invasive Surgery and rtPA for Intracerebral Hemorrhage EvacuationCompletedNCT00224770Phase 2
2A Pilot Study of Inpatient Hospice With Procurement of Brain Tumor Tissue on Expiration for Research PurposesTerminatedNCT01251913

Search NIH Clinical Center for Cerebritis

Genetic Tests for Cerebritis

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Anatomical Context for Cerebritis

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MalaCards organs/tissues related to Cerebritis:

33
Breast, Lung, Brain, Bone, T cells, Endothelial, Liver

Animal Models for Cerebritis or affiliated genes

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MGI Mouse Phenotypes related to Cerebritis:

38
idDescriptionMGI Source AccessionScoreTop Affiliating Genes
1MP:00053817.8AQP4, CASP3, DNM2, GFAP, TNF, TNFRSF1B
2MP:00053977.1AQP4, CASP3, CFB, GRIA1, IRAK4, MUC5B
3MP:00053847.0CASP3, DNM2, GFAP, IRAK4, MUC5B, PRTN3
4MP:00053857.0AQP4, CASP3, DNM2, GFAP, GSR, SETD2
5MP:00053866.8AQP4, CASP3, GFAP, GRIA1, GRIK1, GRIK2
6MP:00053876.5AQP4, CASP3, CFB, GFAP, IRAK4, MUC5B
7MP:00036316.5AQP4, CASP3, DNM2, GFAP, GRIA1, GRIK1
8MP:00053785.8AQP4, CASP3, DNM2, GFAP, GRIA1, GRIK1

Publications for Cerebritis

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Articles related to Cerebritis:

(show top 50)    (show all 13193)
idTitleAuthorsYear
1
The gender-specific association of CXCL16 A181V gene polymorphism with susceptibility to multiple sclerosis, and its effects on PBMC mRNA and plasma soluble CXCL16 levels: preliminary findings. (24854635)
2014
2
Mumps outbreak in the Federation of Bosnia and Herzegovina with large cohorts of susceptibles and genetically diverse strains of genotype G, Bosnia and Herzegovina, December 2010 to September 2012. (25166347)
2014
3
Bullous pemphigoid: associations and management guidelines: facts and controversies. (23806157)
2013
4
Presternal dermoid cyst mimicking lymphatic malformation: a case report and review of the literature. (23163867)
2013
5
Case of the month. Multiple odontogenic keratocysts in association with nevoid basal cell carcinoma syndrome (NBCCS). (24400412)
2013
6
A case of Hickam's dictum: concurrent appendicitis and ectopic pregnancy. (23993940)
2013
7
Mogamulizumab for the treatment of adult T-cell leukemia/lymphoma. (23110261)
2012
8
The human MSH5 (MutSHomolog 5) protein localizes to mitochondria and protects the mitochondrial genome from oxidative damage. (22917773)
2012
9
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management. (22889154)
2012
10
Superficial siderosis associated with multiple dural tears opening into a spinal epidural fluid collection. (21748941)
2011
11
Bilateral pneumothorax in pregnancy unmasking lymphangioleiomyomatosis. (21076889)
2011
12
An aortic root pseudoaneurysm that developed after implantation of a rectus abdominis muscle flap to treat an MRSA mediastinitis: a case report. (20190716)
2010
13
Transcatheter occlusion of patent ductus arteriosus in pre-term infants. (20488412)
2010
14
Phosphorylation status of the NR2B subunit of NMDA receptor regulates its interaction with calcium/calmodulin-dependent protein kinase II. (19453375)
2009
15
Investigation of leucine-rich repeat kinase 2 : enzymological properties and novel assays. (19076219)
2009
16
Giant cell tumor of the thoracic spine: case report and review of the literature. (18207522)
2009
17
Successful treatment of extramedullary gastric plasmacytoma with the combination of bortezomib and dexamethasone: first reported case. (17560647)
2008
18
KRAS mutation in metastatic colorectal cancer and its impact on the use of EGFR inhibitors. (19378369)
2008
19
Rates of infiltration by macrophages and dendritic cells and expression of interleukin-18 and interleukin-12 in the chronic inflammatory lesions of SjAPgren's syndrome: correlation with certain features of immune hyperactivity and factors associated with high risk of lymphoma development. (18050195)
2007
20
Effects of treadmill exercise on dopaminergic transmission in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-lesioned mouse model of basal ganglia injury. (17507552)
2007
21
Family-based association analyses of alcohol dependence phenotypes across DRD2 and neighboring gene ANKK1. (17850642)
2007
22
Aborted sudden cardiac death revealing isolated noncompaction of the left ventricle in a patient with wolff-Parkinson-white syndrome. (17367369)
2007
23
Emergence of sporotrichosis in Manipur. (16912444)
2006
24
Mutational analysis of PRDM1 indicates a tumor-suppressor role in diffuse large B-cell lymphomas. (16424392)
2006
25
Plasmapheresis in acute disseminated encephalomyelitis. (16465015)
2006
26
TNF inhibitors for inflammatory arthritis in New Zealand. (16258581)
2005
27
The zinc finger motif of Escherichia coli RecQ is implicated in both DNA binding and protein folding. (15292213)
2004
28
No evidence for involvement of SDHD in neuroblastoma pathogenesis. (15331017)
2004
29
Luteolysis induced by a gonadotropin-releasing hormone agonist is the key to prevention of ovarian hyperstimulation syndrome. (14711532)
2004
30
Glucuronidation enzymes, genes and psychiatry. (12899737)
2003
31
Myositis ossificans as a complication of a muscle tendon junction strain of long head of biceps. A case report. (12629466)
2003
32
Association between glutathione S-transferase p1 polymorphisms and lung cancer risk in Caucasians: a case-control study. (12660004)
2003
33
Mechanisms of action of nebulized low molecular weights heparin in patients with bronchial asthma]. (15058258)
2003
34
Agnosia for object orientation: naming and mental rotation evidence. (12221142)
2002
35
Single-step assays to analyze CYP2D6 gene polymorphisms in Asians: allele frequencies and a novel *14B allele in mainland Chinese. (12089164)
2002
36
Phosphorylation of isolated human phosphodiesterase-5 regulatory domain induces an apparent conformational change and increases cGMP binding affinity. (12359732)
2002
37
Rapid Notch1 nuclear translocation after ligand binding depends on presenilin-associated gamma-secretase activity. (11193154)
2000
38
Presence of activating transcription factor 4 (ATF4) in the porcine anterior pituitary. (10509809)
1999
39
Angiotensin-converting enzyme deletion polymorphism is associated with hypertension in a Sikh population. (9358012)
1997
40
Stricture and pouchitis after ileal pouch-anal anastomosis. (9407824)
1997
41
Acute and transient psychotic disorder: comorbidity with personality disorder. (9021000)
1996
42
Nuclear transcription factor Oct-1 binds to the 5'-upstream region of CYP1A1 and negatively regulates its expression. (8729008)
1996
43
Serum neuron-specific enolase in human status epilepticus. (7783877)
1995
44
Prevention of urethral stricture recurrence using clean intermittent self-catheterization. (8032838)
1994
45
Overexpression of human lipoprotein lipase in transgenic mice. Resistance to diet-induced hypertriglyceridemia and hypercholesterolemia. (8349676)
1993
46
A beta-spectrin isoform from Drosophila (beta H) is similar in size to vertebrate dystrophin. (2229176)
1990
47
Effects of aspirin and prostaglandin E2 on interdigestive motility complex and duodenogastric reflux in man. (3858090)
1985
48
Prenatal diagnosis of propionic acidemia. (470045)
1979
49
Iodine deficiency in two endemic goiter areas of central and southern Italy. (4160409)
1966
50
CENTRAL PONTINE MYELINOLYSIS. (14200786)
1964

Variations for Cerebritis

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Expression for genes affiliated with Cerebritis

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Search GEO for disease gene expression data for Cerebritis.

Pathways for genes affiliated with Cerebritis

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GO Terms for genes affiliated with Cerebritis

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Biological processes related to Cerebritis according to GeneCards Suite gene sharing:

idNameGO IDScoreTop Affiliating Genes
1histone lysine methylationGO:003496810.3SETD1A, SETD2
2apoptotic signaling pathwayGO:00971909.3CASP3, TNF, TNFRSF1B
3extrinsic apoptotic signaling pathwayGO:00971919.2CASP3, TNF, TNFRSF1B
4response to lipopolysaccharideGO:00324968.5CASP3, CXCL1, CXCL5, TNFRSF1B

Sources for Cerebritis

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2CDC
14ExPASy
15FDA
16FMA
24GTR
25HGMD
26HMDB
27ICD10
28ICD10 via Orphanet
29ICD9CM
30IUPHAR
31KEGG
34MedGen
36MeSH
37MESH via Orphanet
38MGI
41NCI
42NCIt
43NDF-RT
46NINDS
47Novoseek
49OMIM
50OMIM via Orphanet
54PubMed
55QIAGEN
60SNOMED-CT via Orphanet
64Tumor Gene Family of Databases
65UMLS
66UMLS via Orphanet