adrenal adenoma |
Disease ID | 1305 |
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Disease | adrenal adenoma |
Definition | Adrenocortical adenomas are benign tumors of the adrenal cortex. [HPO:probinson, pmid:17287480] |
Synonym | [m]adrenal cortical adenoma nos [m]adrenal cortical adenoma nos (morphologic abnormality) adenoma adrenal adenoma adrenal cortex adenoma adrenal cortical adenoma of adrenal cortex adenoma of adrenal gland adenoma of the adrenal cortex adenoma of the adrenal gland adenoma, adrenal cortical adenoma, adrenocortical adenoma, adrenocortical, benign adenomas adrenal adenomas, adrenal cortical adenomas, adrenocortical adrenal adenoma (disorder) adrenal cortex adenoma adrenal cortex, adenoma adrenal cortical adenoma adrenal cortical adenoma (disorder) adrenal cortical adenoma (morphologic abnormality) adrenal cortical adenoma - morphology adrenal cortical adenoma - morphology (morphologic abnormality) adrenal cortical adenoma morphology adrenal cortical adenoma, no icd-o subtype adrenal cortical adenoma, no icd-o subtype (morphologic abnormality) adrenal cortical adenoma, no international classification of diseases for oncology subtype adrenal cortical adenoma, no international classification of diseases for oncology subtype (morphologic abnormality) adrenal cortical adenoma, nos adrenal cortical adenomas adrenal gland adenoma adrenocortical adenoma adrenocortical adenoma [disease/finding] adrenocortical adenomas benign adenoma of adrenal gland benign adenoma of the adrenal gland benign adrenal adenoma benign adrenal gland adenoma cortical cell adenoma |
DOID | |
UMLS | C0206667 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:21) C0010481 | cushing's syndrome | 13 C1384514 | primary aldosteronism | 6 C0010481 | cushing syndrome | 6 C0001622 | hypercortisolism | 5 C0020428 | aldosteronism | 4 C0020538 | hypertension | 4 C1384514 | primary hyperaldosteronism | 3 C0020428 | hyperaldosteronism | 3 C0007134 | renal cell carcinoma | 1 C0007134 | renal carcinoma | 1 C0031511 | adrenal pheochromocytoma | 1 C0079924 | oligohydramnios | 1 C0406810 | carney complex | 1 C0019204 | hepatocellular carcinoma | 1 C1370740 | adrenal carcinoma | 1 C0007134 | renal cell carcinomas | 1 C0003028 | anhidrosis | 1 C0014145 | yolk sac tumour | 1 C0001627 | congenital adrenal hyperplasia | 1 C0001973 | alcoholism | 1 C0031511 | pheochromocytoma | 1 |
Curated Gene | (Waiting for update.) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:119) 79611 | ACSS3 | 2.351 | DISEASES 111 | ADCY5 | 1.615 | DISEASES 9370 | ADIPOQ | 1.501 | DISEASES 183 | AGT | 1.891 | DISEASES 186 | AGTR2 | 1.286 | DISEASES 8644 | AKR1C3 | 1.566 | DISEASES 8644 | AKR1C3 | 1.154 | DISEASES 279 | AMY2A | 1.238 | DISEASES 64333 | ARHGAP9 | 1.872 | DISEASES 444 | ASPH | 2.856 | DISEASES 480 | ATP1A4 | 5.552 | DISEASES 480 | ATP1A4 | 2.717 | DISEASES 10159 | ATP6AP2 | 1.087 | DISEASES 551 | AVP | 1.157 | DISEASES 153571 | C5orf38 | 2.595 | DISEASES 768 | CA9 | 1.296 | DISEASES 8912 | CACNA1H | 3.531 | DISEASES 779 | CACNA1S | 1.369 | DISEASES 57118 | CAMK1D | 1.071 | DISEASES 1188 | CLCNKB | 1.269 | DISEASES 1499 | CTNNB1 | 2.464 | DISEASES 1499 | CTNNB1 | 1.958 | DISEASES 1528 | CYB5A | 2.372 | DISEASES 1528 | CYB5A | 1.796 | DISEASES 1585 | CYP11B2 | 6.577 | DISEASES 1585 | CYP11B2 | 3.846 | DISEASES 1586 | CYP17A1 | 4.1 | DISEASES 1586 | CYP17A1 | 3.35 | DISEASES 1589 | CYP21A2 | 2.88 | DISEASES 1589 | CYP21A2 | 2.326 | DISEASES 1555 | CYP2B6 | 2.507 | DISEASES 1555 | CYP2B6 | 1.477 | DISEASES 1580 | CYP4B1 | 2.262 | DISEASES 1580 | CYP4B1 | 1.126 | DISEASES 1733 | DIO1 | 1.131 | DISEASES 1781 | DYNC1I2 | 1.642 | DISEASES 1906 | EDN1 | 1.953 | DISEASES 2128 | EVX1 | 1.749 | DISEASES 2248 | FGF3 | 1.389 | DISEASES 90480 | GADD45GIP1 | 1.63 | DISEASES 60674 | GAS5 | 1.78 | DISEASES 2695 | GIP | 2.213 | DISEASES 2695 | GIP | 2.164 | DISEASES 2696 | GIPR | 2.637 | DISEASES 2696 | GIPR | 1.604 | DISEASES 2778 | GNAS | 1.225 | DISEASES 2868 | GRK4 | 2.25 | DISEASES 2938 | GSTA1 | 1.349 | DISEASES 9464 | HAND2 | 1.986 | DISEASES 9464 | HAND2 | 1.83 | DISEASES 100316868 | HOTTIP | 1.216 | DISEASES 285943 | HOXA-AS2 | 2.062 | DISEASES 3283 | HSD3B1 | 3.324 | DISEASES 3283 | HSD3B1 | 2.797 | DISEASES 3284 | HSD3B2 | 2.864 | DISEASES 3284 | HSD3B2 | 2.086 | DISEASES 3360 | HTR4 | 2.811 | DISEASES 3360 | HTR4 | 1.03 | DISEASES 3481 | IGF2 | 2.441 | DISEASES 3481 | IGF2 | 2.156 | DISEASES 3645 | INSRR | 2.455 | DISEASES 3762 | KCNJ5 | 6.352 | DISEASES 3762 | KCNJ5 | 2.228 | DISEASES 3775 | KCNK1 | 1.254 | DISEASES 8645 | KCNK5 | 2.101 | DISEASES 3778 | KCNMA1 | 1.017 | DISEASES 10984 | KCNQ1OT1 | 1.64 | DISEASES 22944 | KIN | 1.249 | DISEASES 9622 | KLK4 | 3.503 | DISEASES 987 | LRBA | 1.175 | DISEASES 126364 | LRRC25 | 1.172 | DISEASES 4158 | MC2R | 3.443 | DISEASES 4158 | MC2R | 2.561 | DISEASES 4221 | MEN1 | 3.703 | DISEASES 4221 | MEN1 | 3.203 | DISEASES 4288 | MKI67 | 1.144 | DISEASES 2315 | MLANA | 3.68 | DISEASES 2315 | MLANA | 2.703 | DISEASES 4311 | MME | 2.11 | DISEASES 4702 | NDUFA8 | 2.291 | DISEASES 255743 | NPNT | 1.515 | DISEASES 4878 | NPPA | 2.948 | DISEASES 190 | NR0B1 | 1.645 | DISEASES 4306 | NR3C2 | 5.502 | DISEASES 3164 | NR4A1 | 1.315 | DISEASES 4929 | NR4A2 | 2.691 | DISEASES 2516 | NR5A1 | 3.834 | DISEASES 2516 | NR5A1 | 3.151 | DISEASES 100169750 | PRINS | 2.201 | DISEASES 100169750 | PRINS | 1.065 | DISEASES 5573 | PRKAR1A | 3.345 | DISEASES 5573 | PRKAR1A | 3.166 | DISEASES 5575 | PRKAR1B | 2.844 | DISEASES 5706 | PSMC6 | 1.162 | DISEASES 389362 | PSMG4 | 2.308 | DISEASES 64783 | RBM15 | 1.931 | DISEASES 6241 | RRM2 | 1.024 | DISEASES 6338 | SCNN1B | 2.276 | DISEASES 6390 | SDHB | 1.596 | DISEASES 6391 | SDHC | 1.769 | DISEASES 6559 | SLC12A3 | 2.173 | DISEASES 57419 | SLC24A3 | 1.622 | DISEASES 1811 | SLC26A3 | 1.03 | DISEASES 2030 | SLC29A1 | 1.14 | DISEASES 23583 | SMUG1 | 1.755 | DISEASES 23583 | SMUG1 | 1.504 | DISEASES 23013 | SPEN | 1.305 | DISEASES 8859 | STK19 | 1.485 | DISEASES 8428 | STK24 | 1.315 | DISEASES 27347 | STK39 | 1.382 | DISEASES 7341 | SUMO1 | 1.051 | DISEASES 6898 | TAT | 1.017 | DISEASES 79718 | TBL1XR1 | 1.89 | DISEASES 10732 | TCFL5 | 1.195 | DISEASES 10178 | TENM1 | 1.026 | DISEASES 7329 | UBE2I | 1.458 | DISEASES 7432 | VIP | 1.156 | DISEASES 7539 | ZFP37 | 2.395 | DISEASES 653808 | ZG16 | 2.827 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1305 |
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Disease | adrenal adenoma |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:20) HP:0001578 | Hypercortisolism | 13 HP:0000822 | Hypertension | 4 HP:0011736 | Primary hyperaldosteronism | 3 HP:0000859 | Mineralocorticoid excess | 3 HP:0009726 | Renal neoplasm | 2 HP:0005584 | Renal cell carcinoma | 2 HP:0007459 | Generalized inability to sweat | 1 HP:0002664 | Neoplasia | 1 HP:0006748 | Adrenal pheochromocytoma | 1 HP:0001402 | Hepatocellular carcinoma | 1 HP:0011742 | Ectopic adrenal gland | 1 HP:0001562 | Oligohydramnios | 1 HP:0000970 | Lack of sweating | 1 HP:0100570 | Carcinoid tumor | 1 HP:0008258 | Congenital adrenal hyperplasia | 1 HP:0006744 | Adrenal carcinoma | 1 HP:0002900 | Hypokalemia | 1 HP:0002721 | Immunodeficiency | 1 HP:0002666 | Pheochromocytoma | 1 HP:0200058 | Angiosarcoma | 1 |
Disease ID | 1305 |
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Disease | adrenal adenoma |
Manually Symptom | UMLS | Name(Total Manually Symptoms:10) |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:8) C1384514 | primary aldosteronism | 7 C0010481 | cushing's syndrome | 6 C0020538 | hypertension | 4 C0010481 | cushing syndrome | 4 C0020428 | hyperaldosteronism | 3 C0001622 | hypercortisolism | 3 C1609519 | adrenal myelolipoma | 1 C0031511 | pheochromocytoma | 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:1) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs76865936 | 18559625 | 50940 | PDE11A | umls:C0206667 | BeFree | One PDE11A inactivating mutation (R307X) was found in one ACA, 22 germ-line missense variants (18.8%) were found in adrenocortical tumors, and only 11 missense variants (5.7%) were found in controls. | 0.002909916 | 2008 | PDE11A | 2 | 178014457 | G | 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 | 1305 |
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Disease | adrenal adenoma |
Case | (Waiting for update.) |