hepatocellular adenoma |
Disease ID | 761 |
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Disease | hepatocellular adenoma |
Definition | A benign epithelial tumor of the LIVER. |
Synonym | adenoma liver adenoma of liver adenoma of liver (disorder) adenoma of liver cells adenoma of the liver cells adenoma, hepatocellular adenoma, hepatocellular, benign adenoma, liver cell adenoma, liver cell [disease/finding] adenomas hepatic adenomas liver adenomas, hepatocellular adenomas, liver cell benign hepatoma benign hepatomas hca hca - hepatocellular adenoma hepatic adenoma hepatocellular adenoma hepatocellular adenomas hepatoma, benign hepatomas, benign liver adenoma liver adenomas liver cell adenoma liver cell adenoma (morphologic abnormality) liver cell adenomas |
Orphanet | |
DOID | |
UMLS | C0206669 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:24) C0017919 | glycogen storage disease | 6 C0019204 | hepatocellular carcinoma | 5 C0017920 | glycogen storage disease type i | 2 C0028754 | obesity | 1 C0006142 | breast cancer | 1 C0032580 | familial adenomatous polyposis coli | 1 C0011847 | diabetes | 1 C0023903 | liver neoplasms | 1 C1956097 | wolf-hirschhorn syndrome | 1 C0032580 | polyposis coli | 1 C0032580 | familial adenomatous polyposis | 1 C0153676 | lung metastasis | 1 C0342276 | maturity-onset diabetes of the young | 1 C0032580 | adenomatous polyposis coli | 1 C0022679 | cystic kidney | 1 C0008313 | sclerosing cholangitis | 1 C0032580 | adenomatous polyposis | 1 C0002871 | anemia | 1 C0022658 | kidney disease | 1 C1384514 | conn syndrome | 1 C0566602 | primary sclerosing cholangitis | 1 C0017920 | type i glycogen storage disease | 1 C0011860 | maturity-onset diabetes | 1 C0023903 | liver tumor | 1 |
Curated Gene | Entrez_id | Symbol | Resource(Total Genes:5) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:49) 174 | AFP | 2.538 | DISEASES 284 | ANGPT1 | 2.024 | DISEASES 56899 | ANKS1B | 2.734 | DISEASES 27237 | ARHGEF16 | 1.93 | DISEASES 55870 | ASH1L | 2.471 | DISEASES 1029 | CDKN2A | 1.276 | DISEASES 1192 | CLIC1 | 1.885 | DISEASES 1499 | CTNNB1 | 5.02 | DISEASES 1543 | CYP1A1 | 2.991 | DISEASES 1544 | CYP1A2 | 3.376 | DISEASES 1555 | CYP2B6 | 2.632 | DISEASES 1576 | CYP3A4 | 1.493 | DISEASES 1629 | DBT | 1.747 | DISEASES 1786 | DNMT1 | 1.62 | DISEASES 8661 | EIF3A | 1.067 | DISEASES 1995 | ELAVL3 | 1.035 | DISEASES 957 | ENTPD5 | 2.335 | DISEASES 7957 | EPM2A | 1.028 | DISEASES 2564 | GABRE | 2.298 | DISEASES 2632 | GBE1 | 1.331 | DISEASES 728441 | GGT2 | 1.43 | DISEASES 2778 | GNAS | 1.435 | DISEASES 51280 | GOLM1 | 1.3 | DISEASES 54865 | GPATCH4 | 3.602 | DISEASES 2719 | GPC3 | 4.018 | DISEASES 2950 | GSTP1 | 2.112 | DISEASES 2996 | GYPE | 1.216 | DISEASES 10767 | HBS1L | 1.7 | DISEASES 3572 | IL6ST | 3.961 | DISEASES 128239 | IQGAP3 | 2.635 | DISEASES 3880 | KRT19 | 2.063 | DISEASES 3855 | KRT7 | 2.048 | DISEASES 51085 | MLXIPL | 1.219 | DISEASES 8856 | NR1I2 | 2.017 | DISEASES 9970 | NR1I3 | 2.666 | DISEASES 4521 | NUDT1 | 1.378 | DISEASES 90780 | PYGO2 | 2.308 | DISEASES 11186 | RASSF1 | 2.543 | DISEASES 83593 | RASSF5 | 2.012 | DISEASES 6191 | RPS4X | 2.522 | DISEASES 6288 | SAA1 | 2.054 | DISEASES 6319 | SCD | 1.566 | DISEASES 4891 | SLC11A2 | 1.088 | DISEASES 1811 | SLC26A3 | 1.053 | DISEASES 23583 | SMUG1 | 1.108 | DISEASES 26771 | SNORD102 | 3.33 | DISEASES 6720 | SREBF1 | 1.082 | DISEASES 8801 | SUCLG2 | 1.366 | DISEASES 23304 | UBR2 | 2.81 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 761 |
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Disease | hepatocellular adenoma |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:11) HP:0001402 | Hepatocellular carcinoma | 5 HP:0030731 | Carcinoma | 4 HP:0002612 | Congenital hepatic fibrosis | 1 HP:0003002 | Breast carcinoma | 1 HP:0004904 | Maturity-onset diabetes of the young | 1 HP:0002896 | Liver cancer | 1 HP:0002664 | Neoplasia | 1 HP:0001903 | Anemia | 1 HP:0000113 | Polycystic kidney dysplasia | 1 HP:0001395 | Hepatic fibrosis | 1 HP:0001513 | Obesity | 1 |
Disease ID | 761 |
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Disease | hepatocellular adenoma |
Manually Symptom | UMLS | Name(Total Manually Symptoms:2) |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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(Waiting for update.) |
All Snps(Total Genotypes:3) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs28934571 | 16799619 | 7157 | TP53 | umls:C0206669 | BeFree | It includes integration of hepatitis B virus (HBV) DNA, R249S TP53 (tumor protein p53) mutation in aflatoxin B1-exposed patients, KRAS mutations related to vinyl chloride exposure, hepatocyte nuclear factor 1alpha (HNF1alpha) mutations associated to hepatocellular adenomas and adenomatosis polyposis coli (APC) germline mutations predisposing to hepatoblastomas. | 0.002909916 | 2006 | TP53 | 17 | 7674216 | C | A |
rs28934571 | 16799619 | 324 | APC | umls:C0206669 | BeFree | It includes integration of hepatitis B virus (HBV) DNA, R249S TP53 (tumor protein p53) mutation in aflatoxin B1-exposed patients, KRAS mutations related to vinyl chloride exposure, hepatocyte nuclear factor 1alpha (HNF1alpha) mutations associated to hepatocellular adenomas and adenomatosis polyposis coli (APC) germline mutations predisposing to hepatoblastomas. | 0.000271442 | 2006 | TP53 | 17 | 7674216 | C | A |
rs28934571 | 16799619 | 3845 | KRAS | umls:C0206669 | BeFree | It includes integration of hepatitis B virus (HBV) DNA, R249S TP53 (tumor protein p53) mutation in aflatoxin B1-exposed patients, KRAS mutations related to vinyl chloride exposure, hepatocyte nuclear factor 1alpha (HNF1alpha) mutations associated to hepatocellular adenomas and adenomatosis polyposis coli (APC) germline mutations predisposing to hepatoblastomas. | 0.000271442 | 2006 | TP53 | 17 | 7674216 | C | A |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Disease ID | 761 |
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Disease | hepatocellular adenoma |
Case | (Waiting for update.) |