MCID: ADN017
MIFTS: 28

Adenofibroma malady

Category: Cancer diseases

Aliases & Classifications for Adenofibroma

About this section

Aliases & Descriptions for Adenofibroma:

Name: Adenofibroma 10 47 12 36 65
 
Adenofibroma, No Icd-O Subtype 10

Classifications:



External Ids:

Disease Ontology10 DOID:2683
MeSH36 D000232
SNOMED-CT59 189823009, 2962009
NCIt42 C8984
UMLS65 C0001422

Summaries for Adenofibroma

About this section
Disease Ontology:10 A cell type benign neoplasm that is composed of glandular and fibrous tissues, with a relatively large proportion of glands.

MalaCards based summary: Adenofibroma, also known as adenofibroma, no icd-o subtype, is related to nephrogenic adenofibroma and uterine corpus adenofibroma. An important gene associated with Adenofibroma is MME (Membrane Metallo-Endopeptidase). Affiliated tissues include brain, lung and breast, and related mouse phenotype liver/biliary system.

Related Diseases for Adenofibroma

About this section

Diseases in the Adenofibroma family:

Malignant Adenofibroma

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

(show top 50)    (show all 122)
idRelated DiseaseScoreTop Affiliating Genes
1nephrogenic adenofibroma12.3
2uterine corpus adenofibroma12.3
3mucinous adenofibroma12.3
4ovarian serous adenofibroma12.3
5ovarian endometrioid adenofibroma12.3
6ovarian clear cell adenofibroma12.3
7ovarian mucinous adenofibroma12.3
8cervical adenofibroma12.2
9clear cell adenofibroma12.2
10fallopian tube adenofibroma12.2
11papillary adenofibroma12.2
12malignant adenofibroma12.2
13ovarian mucinous malignant adenofibroma12.2
14ovarian endometrioid malignant adenofibroma12.2
15ovarian clear cell malignant adenofibroma12.2
16giant adenofibroma of the breast12.2
17cystadenofibroma10.4
18breast cancer10.3
19spermatocytoma10.3INHA, MME
20endometrial mucinous adenocarcinoma10.2INHA, MME
21ovarian brenner tumor10.2INHA, MME
22prostate cancer10.2
23atherosclerosis10.2
24hepatitis10.2
25hydrocephalus10.2
26leukemia10.2
27lymphoma10.2
28prostatitis10.2
29thyroiditis10.2
30thymus lipoma10.2ARID1A, MME
31mucinous tubular and spindle renal cell carcinoma10.1HNF1B, MME
32fasciitis10.1HNF1B, INHA
33hilar cholangiocellular carcinoma10.1INHA, MME
34uterine corpus endometrial stromal sarcoma10.1INHA, MME
35rheumatoid arthritis10.0
36neuroblastoma10.0
37colorectal cancer10.0
38hiv-110.0
39alcohol dependence10.0
40leprosy10.0
41smith-lemli-opitz syndrome10.0
42retinoblastoma10.0
43digeorge syndrome10.0
44acute monocytic leukemia10.0
45alopecia10.0
46arthritis10.0
47b-cell lymphomas10.0
48burn scar10.0
49burns10.0
50glomerulonephritis10.0

Graphical network of the top 20 diseases related to Adenofibroma:



Diseases related to adenofibroma

Symptoms for Adenofibroma

About this section

Drugs & Therapeutics for Adenofibroma

About this section

Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Adenofibroma


Cochrane evidence based reviews: adenofibroma

Genetic Tests for Adenofibroma

About this section

Anatomical Context for Adenofibroma

About this section

MalaCards organs/tissues related to Adenofibroma:

33
Brain, Lung, Breast, Prostate, B cells, T cells, Monocytes

Animal Models for Adenofibroma or affiliated genes

About this section

MGI Mouse Phenotypes related to Adenofibroma:

38
idDescriptionMGI Source AccessionScoreTop Affiliating Genes
1MP:00053708.7BRAF, HNF1B, INHA, MME

Publications for Adenofibroma

About this section

Articles related to Adenofibroma:

(show top 50)    (show all 104)
idTitleAuthorsYear
1
Frequency and causes of C-reactive protein and erythrocyte sedimentation rate disagreements in adults. (25594234)
2015
2
Increased leukemia-associated gene expression in benzene-exposed workers. (24993241)
2014
3
Antiparallel triple-strand architecture for prefibrillar AI^42 oligomers. (25118290)
2014
4
Williams syndrome: a case series. (24953591)
2014
5
Posterior polymorphous corneal dystrophy 3 is associated with agenesis and hypoplasia of the corpus callosum. (24780443)
2014
6
Successful autologous cord blood transplantation in a child with acquired severe aplastic anemia. (23464883)
2013
7
Ruxolitinib for myelofibrosis--an update of its clinical effects. (24238036)
2013
8
Microglial proliferation in the brain of chronic alcoholics with hepatic encephalopathy. (24346482)
2013
9
Perceived occupational exposures of home care workers and the association to general tension, shoulder-neck and low back pain. (24004770)
2013
10
Paroxysmal extreme pain disorder. (23599527)
2013
11
Deep infiltrating colorectal endometriosis treated with robotic-assisted rectosigmoidectomy. (23925016)
2013
12
Lack of association between C3123A polymorphism of the angiotensin II type 2 receptor gene and hypertension in Tunisian population. (22987376)
2012
13
An atypical facial appearance and growth pattern in a child with Cornelia de Lange Syndrome: an intragenic deletion predicting loss of the N-terminal region of NIPBL. (21934607)
2012
14
Treatment of cherubism with salmon calcitonin: a case report. (21912506)
2011
15
Late-onset endophthalmitis secondary to exposed glaucoma tube implant in a rare case of paediatric glaucoma. (22611505)
2011
16
Centrally administered relaxin-3 induces Fos expression in the osmosensitive areas in rat brain and facilitates water intake. (20214940)
2010
17
Clinical improvement in patients with autosomal recessive pseudohypoaldosteronism and the necessity for salt supplementation. (20661616)
2010
18
Proteinase-activated receptor-2 activation evokes oesophageal longitudinal smooth muscle contraction via a capsaicin-sensitive and neurokinin-2 receptor-dependent pathway. (19740117)
2010
19
Multimodality evaluation of intracranial vasodilatory reserve in carotid artery disease. (19548339)
2009
20
Coordinate control of expression of Nrf2-modulated genes in the human small airway epithelium is highly responsive to cigarette smoking. (19593404)
2009
21
Unilateral multicystic dysplastic kidney: a meta-analysis of observational studies on the incidence, associated urinary tract malformations and the contralateral kidney. (19171687)
2009
22
Silent sinus syndrome with spontaneous orbital floor reconstruction. (19670601)
2009
23
Pax6 promotes neurogenesis in human neural stem cells. (18595732)
2008
24
Fibrinogen gene variation and ischemic stroke. (18331453)
2008
25
Activation of protein kinase Cepsilon stimulates DNA-repair via epidermal growth factor receptor nuclear accumulation. (18037521)
2008
26
Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia. (17961261)
2007
27
Hydrolytic metabolism of pyrethroids by human and other mammalian carboxylesterases. (16387282)
2006
28
Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12. (16574454)
2006
29
Recurrent acute pancreatitis due to a hydatid cyst of the pancreatic head: a case report and review of the literature. (16006687)
2005
30
Thrombophilia and fetal growth restriction. (15036708)
2004
31
Beta-catenin antisense studies in embryonic liver cultures: role in proliferation, apoptosis, and lineage specification. (12512043)
2003
32
A set of Hox proteins interact with the Maf oncoprotein to inhibit its DNA binding, transactivation, and transforming activities. (11036080)
2001
33
Developmental dyscalculia is a familial learning disability. (15497272)
2001
34
Deep intralobular extension of human hepatic 'progenitor cells' correlates with parenchymal inflammation in chronic viral hepatitis: can 'progenitor cells' migrate? (11054721)
2000
35
Human galectin-3 is a novel chemoattractant for monocytes and macrophages. (10925302)
2000
36
Intravenous epoprostenol: a new therapy for primary pulmonary hypertension. (11878257)
2000
37
Investigation of nonimmune hydrops fetalis: multidisciplinary studies are necessary for diagnosis--review of 94 cases. (10441620)
1999
38
Nonimmune hydrops fetalis. (10818859)
1999
39
Vascular nitric oxide, sex hormone replacement, and fish oil may help to prevent Alzheimer's disease by suppressing synthesis of acute-phase cytokines. (10616034)
1999
40
Defective IL7R expression in T(-)B(+)NK(+) severe combined immunodeficiency. (9843216)
1998
41
Genotypic variation in the transforming growth factor-beta1 gene: association with transforming growth factor-beta1 production, fibrotic lung disease, and graft fibrosis after lung transplantation. (9808485)
1998
42
Gene amplifications in advanced-stage human prostate cancer. (7740653)
1995
43
Pyridostigmine induced growth hormone release in mania: focus on the cholinergic/somatostatin system. (8306487)
1994
44
Expression of p53 protein in gastric carcinomas is not independently prognostic. (7940194)
1994
45
The tissue distribution of factor XIIIa positive cells. (8095915)
1993
46
Ten novel mutations in the HEXA gene in non-Jewish Tay-Sachs patients. (8490625)
1993
47
Human papillomavirus type 16 DNA in oesophageal squamous cell carcinoma. (8297121)
1993
48
Phase II trial of recombinant tumor necrosis factor in disseminated malignant melanoma. (1590281)
1992
49
The modulation of ferryl myoglobin formation and its oxidative effects on low density lipoproteins by nitric oxide. (1743289)
1991
50
A comparative evaluation of the safety and efficacy of cefotetan and cefoxitin in surgical prophylaxis. (2008777)
1991

Variations for Adenofibroma

About this section

Expression for genes affiliated with Adenofibroma

About this section
Search GEO for disease gene expression data for Adenofibroma.

Pathways for genes affiliated with Adenofibroma

About this section

GO Terms for genes affiliated with Adenofibroma

About this section

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

idNameGO IDScoreTop Affiliating Genes
1Notch signaling pathwayGO:00072199.0HNF1B, MAML2

Sources for Adenofibroma

About this section
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