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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   adrenal adenoma
  

Disease ID 1305
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
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
Disease adrenal adenoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:10)
C2609073  |  splenic peliosis
C2118097  |  agonadism
C1963138  |  hypertension
C1608408  |  malignant transformation
C1384514  |  primary aldosteronism
C0042755  |  virilism
C0020428  |  hyperaldosteronism
C0010481  |  hypercortisolism
C0010481  |  cushing syndrome
C0001622  |  hypercorticism
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)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs768659361855962550940PDE11Aumls:C0206667BeFreeOne 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.0.0029099162008PDE11A2178014457GA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Disease ID 1305
Disease adrenal adenoma
Case(Waiting for update.)