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Pediatric Disease Annotations & Medicines



   adrenal cortical carcinoma
  

Disease ID 824
Disease adrenal cortical carcinoma
Definition
A malignant neoplasm of the adrenal cortex that may produce hormones such as cortisol, aldosterone, estrogen, or testosterone. [HPO:probinson]
Synonym
adenocarcinoma adrenal
adenocarcinoma, adrenocortical, malignant
adrenal adenocarcinoma
adrenal carcinoma
adrenal carcinoma (disorder)
adrenal carcinomas
adrenal cortex adenocarcinoma
adrenal cortex cancer
adrenal cortex cancer, carcinoma
adrenal cortex carcinoma
adrenal cortex, carcinoma
adrenal cortical adenocarcinoma
adrenal cortical carcinoma (morphologic abnormality)
adrenal cortical carcinomas
adrenal gland carinoma
adrenocortical cancer
adrenocortical carcinoma
adrenocortical carcinoma [disease/finding]
adrenocortical carcinoma, nos
adrenocortical carcinomas
cancer of the adrenal cortex
carcinoma adrenal
carcinoma of adrenal cortex
carcinoma of the adrenal cortex
carcinoma, adrenal cortical
carcinoma, adrenocortical
carcinoma, adrenocortical, malignant
carcinomas, adrenal cortical
carcinomas, adrenocortical
cortical cell carcinoma
Orphanet
DOID
UMLS
C0206686
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:18)
C0153676  |  pulmonary metastases  |  2
C0040053  |  thrombus  |  2
C0221002  |  primary hyperparathyroidism  |  1
C0406810  |  carney complex  |  1
C0019204  |  hepatocellular carcinoma  |  1
C0010481  |  cushing's syndrome  |  1
C0494165  |  liver metastasis  |  1
C1621895  |  adrenal hyperplasia  |  1
C0020428  |  aldosteronism  |  1
C0206081  |  hyperandrogenism  |  1
C0031511  |  pheochromocytomas  |  1
C0020502  |  hyperparathyroidism  |  1
C0001627  |  congenital adrenal hyperplasia  |  1
C0334684  |  renal adenoma  |  1
C1384514  |  primary aldosteronism  |  1
C0027708  |  wilms tumor  |  1
C0206667  |  adrenal adenoma  |  1
C0018801  |  heart failure  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:17)
ABCB1  |  5243  |  CTD_human
TP53  |  7157  |  CTD_human;ORPHANET
IGF2  |  3481  |  CTD_human
TOP2A  |  7153  |  CTD_human
MED12  |  9968  |  CTD_human
IGF1R  |  3480  |  CTD_human
TERT  |  7015  |  CTD_human
BRAF  |  673  |  CTD_human
CDKN2A  |  1029  |  CTD_human
CTNNB1  |  1499  |  CTD_human
EGFR  |  1956  |  CTD_human
SPARC  |  6678  |  CTD_human
RRM1  |  6240  |  CTD_human
RB1  |  5925  |  CTD_human
MEN1  |  4221  |  CTD_human
DAXX  |  1616  |  CTD_human
ZNRF3  |  84133  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:457)
3675  |  ITGA3  |  DISEASES
3675  |  ITGA3  |  DISEASES
2067  |  ERCC1  |  DISEASES
2067  |  ERCC1  |  DISEASES
2896  |  GRN  |  DISEASES
2249  |  FGF4  |  DISEASES
27231  |  NMRK2  |  DISEASES
27231  |  NMRK2  |  DISEASES
4680  |  CEACAM6  |  DISEASES
1071  |  CETP  |  DISEASES
4504  |  MT3  |  DISEASES
4504  |  MT3  |  DISEASES
7051  |  TGM1  |  DISEASES
124  |  ADH1A  |  DISEASES
124  |  ADH1A  |  DISEASES
83933  |  HDAC10  |  DISEASES
1113  |  CHGA  |  DISEASES
1113  |  CHGA  |  DISEASES
1666  |  DECR1  |  DISEASES
81576  |  CCDC130  |  DISEASES
8529  |  CYP4F2  |  DISEASES
8529  |  CYP4F2  |  DISEASES
6822  |  SULT2A1  |  DISEASES
6822  |  SULT2A1  |  DISEASES
6822  |  SULT2A1  |  DISEASES
5919  |  RARRES2  |  DISEASES
5919  |  RARRES2  |  DISEASES
7431  |  VIM  |  DISEASES
5216  |  PFN1  |  DISEASES
5216  |  PFN1  |  DISEASES
2026  |  ENO2  |  DISEASES
2026  |  ENO2  |  DISEASES
2690  |  GHR  |  DISEASES
2908  |  NR3C1  |  DISEASES
3485  |  IGFBP2  |  DISEASES
3485  |  IGFBP2  |  DISEASES
6943  |  TCF21  |  DISEASES
6943  |  TCF21  |  DISEASES
79646  |  PANK3  |  DISEASES
6909  |  TBX2  |  DISEASES
6909  |  TBX2  |  DISEASES
23397  |  NCAPH  |  DISEASES
2693  |  GHSR  |  DISEASES
2693  |  GHSR  |  DISEASES
4656  |  MYOG  |  DISEASES
79365  |  BHLHE41  |  DISEASES
79365  |  BHLHE41  |  DISEASES
8082  |  SSPN  |  DISEASES
3598  |  IL13RA2  |  DISEASES
3598  |  IL13RA2  |  DISEASES
3623  |  INHA  |  DISEASES
3623  |  INHA  |  DISEASES
7389  |  UROD  |  DISEASES
29108  |  PYCARD  |  DISEASES
7103  |  TSPAN8  |  DISEASES
3976  |  LIF  |  DISEASES
3630  |  INS  |  DISEASES
3630  |  INS  |  DISEASES
4298  |  MLLT1  |  DISEASES
9253  |  NUMBL  |  DISEASES
1327  |  COX4I1  |  DISEASES
1327  |  COX4I1  |  DISEASES
2488  |  FSHB  |  DISEASES
2488  |  FSHB  |  DISEASES
7014  |  TERF2  |  DISEASES
7014  |  TERF2  |  DISEASES
182  |  JAG1  |  DISEASES
182  |  JAG1  |  DISEASES
891  |  CCNB1  |  DISEASES
8536  |  CAMK1  |  DISEASES
8536  |  CAMK1  |  DISEASES
10542  |  LAMTOR5  |  DISEASES
10542  |  LAMTOR5  |  DISEASES
377  |  ARF3  |  DISEASES
967  |  CD63  |  DISEASES
4856  |  NOV  |  DISEASES
4856  |  NOV  |  DISEASES
2230  |  FDX1  |  DISEASES
2230  |  FDX1  |  DISEASES
2230  |  FDX1  |  DISEASES
1588  |  CYP19A1  |  DISEASES
1588  |  CYP19A1  |  DISEASES
1588  |  CYP19A1  |  DISEASES
9360  |  PPIG  |  DISEASES
9360  |  PPIG  |  DISEASES
9194  |  SLC16A7  |  DISEASES
9194  |  SLC16A7  |  DISEASES
11019  |  LIAS  |  DISEASES
11019  |  LIAS  |  DISEASES
11019  |  LIAS  |  DISEASES
23326  |  USP22  |  DISEASES
23326  |  USP22  |  DISEASES
7434  |  VIPR2  |  DISEASES
7434  |  VIPR2  |  DISEASES
23678  |  SGK3  |  DISEASES
23678  |  SGK3  |  DISEASES
1387  |  CREBBP  |  DISEASES
5595  |  MAPK3  |  DISEASES
22858  |  ICK  |  DISEASES
6855  |  SYP  |  DISEASES
6855  |  SYP  |  DISEASES
3977  |  LIFR  |  DISEASES
3791  |  KDR  |  DISEASES
3791  |  KDR  |  DISEASES
867  |  CBL  |  DISEASES
2247  |  FGF2  |  DISEASES
5443  |  POMC  |  DISEASES
5443  |  POMC  |  DISEASES
5443  |  POMC  |  DISEASES
10723  |  SLC12A7  |  DISEASES
10723  |  SLC12A7  |  DISEASES
1950  |  EGF  |  DISEASES
7472  |  WNT2  |  DISEASES
25824  |  PRDX5  |  DISEASES
25824  |  PRDX5  |  DISEASES
1616  |  DAXX  |  DISEASES
1616  |  DAXX  |  DISEASES
22822  |  PHLDA1  |  DISEASES
22822  |  PHLDA1  |  DISEASES
6895  |  TARBP2  |  DISEASES
6895  |  TARBP2  |  DISEASES
60314  |  C12orf10  |  DISEASES
60314  |  C12orf10  |  DISEASES
3480  |  IGF1R  |  DISEASES
3480  |  IGF1R  |  DISEASES
1583  |  CYP11A1  |  DISEASES
1583  |  CYP11A1  |  DISEASES
1583  |  CYP11A1  |  DISEASES
1000  |  CDH2  |  DISEASES
1000  |  CDH2  |  DISEASES
7157  |  TP53  |  DISEASES
7157  |  TP53  |  DISEASES
7157  |  TP53  |  DISEASES
207  |  AKT1  |  DISEASES
207  |  AKT1  |  DISEASES
8915  |  BCL10  |  DISEASES
375  |  ARF1  |  DISEASES
5972  |  REN  |  DISEASES
5972  |  REN  |  DISEASES
5972  |  REN  |  DISEASES
805  |  CALM2  |  DISEASES
805  |  CALM2  |  DISEASES
1956  |  EGFR  |  DISEASES
1956  |  EGFR  |  DISEASES
6770  |  STAR  |  DISEASES
6770  |  STAR  |  DISEASES
6770  |  STAR  |  DISEASES
1392  |  CRH  |  DISEASES
1392  |  CRH  |  DISEASES
1392  |  CRH  |  DISEASES
133  |  ADM  |  DISEASES
133  |  ADM  |  DISEASES
9049  |  AIP  |  DISEASES
9049  |  AIP  |  DISEASES
5331  |  PLCB3  |  DISEASES
5331  |  PLCB3  |  DISEASES
7108  |  TM7SF2  |  DISEASES
7108  |  TM7SF2  |  DISEASES
150  |  ADRA2A  |  DISEASES
150  |  ADRA2A  |  DISEASES
50940  |  PDE11A  |  DISEASES
50940  |  PDE11A  |  DISEASES
9133  |  CCNB2  |  DISEASES
9133  |  CCNB2  |  DISEASES
808  |  CALM3  |  DISEASES
808  |  CALM3  |  DISEASES
1584  |  CYP11B1  |  DISEASES
1584  |  CYP11B1  |  DISEASES
1584  |  CYP11B1  |  DISEASES
3101  |  HK3  |  DISEASES
3101  |  HK3  |  DISEASES
92304  |  SCGB3A1  |  DISEASES
54165  |  DCUN1D1  |  DISEASES
54165  |  DCUN1D1  |  DISEASES
162417  |  NAGS  |  DISEASES
60675  |  PROK2  |  DISEASES
6997  |  TDGF1  |  DISEASES
308  |  ANXA5  |  DISEASES
308  |  ANXA5  |  DISEASES
84889  |  SLC7A3  |  DISEASES
84889  |  SLC7A3  |  DISEASES
9317  |  PTER  |  DISEASES
9317  |  PTER  |  DISEASES
4108  |  MAGEA9  |  DISEASES
4108  |  MAGEA9  |  DISEASES
717  |  C2  |  DISEASES
717  |  C2  |  DISEASES
6240  |  RRM1  |  DISEASES
6240  |  RRM1  |  DISEASES
1549  |  CYP2A7  |  DISEASES
1549  |  CYP2A7  |  DISEASES
1642  |  DDB1  |  DISEASES
1642  |  DDB1  |  DISEASES
8313  |  AXIN2  |  DISEASES
8313  |  AXIN2  |  DISEASES
3479  |  IGF1  |  DISEASES
3479  |  IGF1  |  DISEASES
3094  |  HINT1  |  DISEASES
3094  |  HINT1  |  DISEASES
3221  |  HOXC4  |  DISEASES
3221  |  HOXC4  |  DISEASES
378  |  ARF4  |  DISEASES
794  |  CALB2  |  DISEASES
794  |  CALB2  |  DISEASES
29785  |  CYP2S1  |  DISEASES
29785  |  CYP2S1  |  DISEASES
3159  |  HMGA1  |  DISEASES
3159  |  HMGA1  |  DISEASES
3159  |  HMGA1  |  DISEASES
9940  |  DLEC1  |  DISEASES
51642  |  MRPL48  |  DISEASES
51642  |  MRPL48  |  DISEASES
572  |  BAD  |  DISEASES
572  |  BAD  |  DISEASES
572  |  BAD  |  DISEASES
7015  |  TERT  |  DISEASES
7015  |  TERT  |  DISEASES
54905  |  CYP2W1  |  DISEASES
54905  |  CYP2W1  |  DISEASES
6578  |  SLCO2A1  |  DISEASES
1240  |  CMKLR1  |  DISEASES
1240  |  CMKLR1  |  DISEASES
55072  |  RNF31  |  DISEASES
55072  |  RNF31  |  DISEASES
4728  |  NDUFS8  |  DISEASES
4728  |  NDUFS8  |  DISEASES
4233  |  MET  |  DISEASES
8630  |  HSD17B6  |  DISEASES
8630  |  HSD17B6  |  DISEASES
8630  |  HSD17B6  |  DISEASES
7262  |  PHLDA2  |  DISEASES
7262  |  PHLDA2  |  DISEASES
2146  |  EZH2  |  DISEASES
2146  |  EZH2  |  DISEASES
2692  |  GHRHR  |  DISEASES
8648  |  NCOA1  |  DISEASES
8648  |  NCOA1  |  DISEASES
84938  |  ATG4C  |  DISEASES
84938  |  ATG4C  |  DISEASES
5179  |  PENK  |  DISEASES
1555  |  CYP2B6  |  DISEASES
1555  |  CYP2B6  |  DISEASES
65985  |  AACS  |  DISEASES
65985  |  AACS  |  DISEASES
1585  |  CYP11B2  |  DISEASES
1585  |  CYP11B2  |  DISEASES
1585  |  CYP11B2  |  DISEASES
221937  |  FOXK1  |  DISEASES
221937  |  FOXK1  |  DISEASES
6667  |  SP1  |  DISEASES
283869  |  NPW  |  DISEASES
283869  |  NPW  |  DISEASES
2831  |  NPBWR1  |  DISEASES
2831  |  NPBWR1  |  DISEASES
83999  |  KREMEN1  |  DISEASES
83999  |  KREMEN1  |  DISEASES
796  |  CALCA  |  DISEASES
220  |  ALDH1A3  |  DISEASES
220  |  ALDH1A3  |  DISEASES
430  |  ASCL2  |  DISEASES
430  |  ASCL2  |  DISEASES
1233  |  CCR4  |  DISEASES
1233  |  CCR4  |  DISEASES
1553  |  CYP2A13  |  DISEASES
1553  |  CYP2A13  |  DISEASES
256933  |  NPB  |  DISEASES
256933  |  NPB  |  DISEASES
4158  |  MC2R  |  DISEASES
4158  |  MC2R  |  DISEASES
8856  |  NR1I2  |  DISEASES
8856  |  NR1I2  |  DISEASES
283  |  ANG  |  DISEASES
4221  |  MEN1  |  DISEASES
4221  |  MEN1  |  DISEASES
4221  |  MEN1  |  DISEASES
1576  |  CYP3A4  |  DISEASES
1576  |  CYP3A4  |  DISEASES
23583  |  SMUG1  |  DISEASES
23583  |  SMUG1  |  DISEASES
3762  |  KCNJ5  |  DISEASES
3762  |  KCNJ5  |  DISEASES
8788  |  DLK1  |  DISEASES
8788  |  DLK1  |  DISEASES
5764  |  PTN  |  DISEASES
1528  |  CYB5A  |  DISEASES
1528  |  CYB5A  |  DISEASES
866  |  SERPINA6  |  DISEASES
866  |  SERPINA6  |  DISEASES
866  |  SERPINA6  |  DISEASES
7874  |  USP7  |  DISEASES
7874  |  USP7  |  DISEASES
10252  |  SPRY1  |  DISEASES
1499  |  CTNNB1  |  DISEASES
1499  |  CTNNB1  |  DISEASES
6146  |  RPL22  |  DISEASES
6146  |  RPL22  |  DISEASES
3899  |  AFF3  |  DISEASES
3899  |  AFF3  |  DISEASES
801  |  CALM1  |  DISEASES
801  |  CALM1  |  DISEASES
11186  |  RASSF1  |  DISEASES
11186  |  RASSF1  |  DISEASES
4111  |  MAGEA12  |  DISEASES
4111  |  MAGEA12  |  DISEASES
6597  |  SMARCA4  |  DISEASES
51170  |  HSD17B11  |  DISEASES
5573  |  PRKAR1A  |  DISEASES
5573  |  PRKAR1A  |  DISEASES
5573  |  PRKAR1A  |  DISEASES
1786  |  DNMT1  |  DISEASES
5575  |  PRKAR1B  |  DISEASES
4311  |  MME  |  DISEASES
4311  |  MME  |  DISEASES
4311  |  MME  |  DISEASES
2475  |  MTOR  |  DISEASES
2475  |  MTOR  |  DISEASES
4536  |  MT-ND2  |  DISEASES
6646  |  SOAT1  |  DISEASES
6646  |  SOAT1  |  DISEASES
4288  |  MKI67  |  DISEASES
6274  |  S100A3  |  DISEASES
6274  |  S100A3  |  DISEASES
262  |  AMD1  |  DISEASES
9900  |  SV2A  |  DISEASES
3283  |  HSD3B1  |  DISEASES
3283  |  HSD3B1  |  DISEASES
3284  |  HSD3B2  |  DISEASES
3284  |  HSD3B2  |  DISEASES
2832  |  NPBWR2  |  DISEASES
2832  |  NPBWR2  |  DISEASES
1586  |  CYP17A1  |  DISEASES
1586  |  CYP17A1  |  DISEASES
1586  |  CYP17A1  |  DISEASES
89885  |  FATE1  |  DISEASES
89885  |  FATE1  |  DISEASES
541466  |  CT45A1  |  DISEASES
541466  |  CT45A1  |  DISEASES
653  |  BMP5  |  DISEASES
653  |  BMP5  |  DISEASES
1557  |  CYP2C19  |  DISEASES
1557  |  CYP2C19  |  DISEASES
7410  |  VAV2  |  DISEASES
7410  |  VAV2  |  DISEASES
1580  |  CYP4B1  |  DISEASES
1580  |  CYP4B1  |  DISEASES
5728  |  PTEN  |  DISEASES
7422  |  VEGFA  |  DISEASES
7422  |  VEGFA  |  DISEASES
5476  |  CTSA  |  DISEASES
6418  |  SET  |  DISEASES
6418  |  SET  |  DISEASES
2516  |  NR5A1  |  DISEASES
2516  |  NR5A1  |  DISEASES
2516  |  NR5A1  |  DISEASES
195828  |  ZNF367  |  DISEASES
195828  |  ZNF367  |  DISEASES
3293  |  HSD17B3  |  DISEASES
3293  |  HSD17B3  |  DISEASES
8242  |  KDM5C  |  DISEASES
8242  |  KDM5C  |  DISEASES
8242  |  KDM5C  |  DISEASES
2159  |  F10  |  DISEASES
1460  |  CSNK2B  |  DISEASES
1460  |  CSNK2B  |  DISEASES
7088  |  TLE1  |  DISEASES
7088  |  TLE1  |  DISEASES
10253  |  SPRY2  |  DISEASES
10253  |  SPRY2  |  DISEASES
10253  |  SPRY2  |  DISEASES
5638  |  PRRG1  |  DISEASES
5638  |  PRRG1  |  DISEASES
1114  |  CHGB  |  DISEASES
1114  |  CHGB  |  DISEASES
190  |  NR0B1  |  DISEASES
190  |  NR0B1  |  DISEASES
190  |  NR0B1  |  DISEASES
1906  |  EDN1  |  DISEASES
1906  |  EDN1  |  DISEASES
3601  |  IL15RA  |  DISEASES
114131  |  UCN3  |  DISEASES
6462  |  SHBG  |  DISEASES
6462  |  SHBG  |  DISEASES
6462  |  SHBG  |  DISEASES
4676  |  NAP1L4  |  DISEASES
4676  |  NAP1L4  |  DISEASES
8644  |  AKR1C3  |  DISEASES
8644  |  AKR1C3  |  DISEASES
8644  |  AKR1C3  |  DISEASES
4267  |  CD99  |  DISEASES
4267  |  CD99  |  DISEASES
2315  |  MLANA  |  DISEASES
2315  |  MLANA  |  DISEASES
2315  |  MLANA  |  DISEASES
2576  |  GAGE4  |  DISEASES
2576  |  GAGE4  |  DISEASES
2543  |  GAGE1  |  DISEASES
2543  |  GAGE1  |  DISEASES
7260  |  TSSC1  |  DISEASES
7260  |  TSSC1  |  DISEASES
2254  |  FGF9  |  DISEASES
2254  |  FGF9  |  DISEASES
6545  |  SLC7A4  |  DISEASES
6545  |  SLC7A4  |  DISEASES
53353  |  LRP1B  |  DISEASES
53353  |  LRP1B  |  DISEASES
7026  |  NR2F2  |  DISEASES
7026  |  NR2F2  |  DISEASES
220963  |  SLC16A9  |  DISEASES
220963  |  SLC16A9  |  DISEASES
79924  |  ADM2  |  DISEASES
79924  |  ADM2  |  DISEASES
30011  |  SH3KBP1  |  DISEASES
30011  |  SH3KBP1  |  DISEASES
30011  |  SH3KBP1  |  DISEASES
344022  |  NOTO  |  DISEASES
344022  |  NOTO  |  DISEASES
221935  |  SDK1  |  DISEASES
221935  |  SDK1  |  DISEASES
6332  |  SCN7A  |  DISEASES
6332  |  SCN7A  |  DISEASES
1385  |  CREB1  |  DISEASES
3481  |  IGF2  |  DISEASES
3481  |  IGF2  |  DISEASES
3481  |  IGF2  |  DISEASES
7849  |  PAX8  |  DISEASES
7849  |  PAX8  |  DISEASES
1589  |  CYP21A2  |  DISEASES
1589  |  CYP21A2  |  DISEASES
1589  |  CYP21A2  |  DISEASES
7153  |  TOP2A  |  DISEASES
7153  |  TOP2A  |  DISEASES
1028  |  CDKN1C  |  DISEASES
1028  |  CDKN1C  |  DISEASES
1028  |  CDKN1C  |  DISEASES
6760  |  SS18  |  DISEASES
6760  |  SS18  |  DISEASES
4193  |  MDM2  |  DISEASES
4193  |  MDM2  |  DISEASES
111  |  ADCY5  |  DISEASES
111  |  ADCY5  |  DISEASES
9404  |  LPXN  |  DISEASES
9404  |  LPXN  |  DISEASES
996  |  CDC27  |  DISEASES
996  |  CDC27  |  DISEASES
6195  |  RPS6KA1  |  DISEASES
51271  |  UBAP1  |  DISEASES
84133  |  ZNRF3  |  DISEASES
84133  |  ZNRF3  |  DISEASES
2232  |  FDXR  |  DISEASES
2232  |  FDXR  |  DISEASES
2232  |  FDXR  |  DISEASES
60674  |  GAS5  |  DISEASES
60674  |  GAS5  |  DISEASES
100169750  |  PRINS  |  DISEASES
100169750  |  PRINS  |  DISEASES
6023  |  RMRP  |  DISEASES
6023  |  RMRP  |  DISEASES
Locus(Waiting for update.)
Disease ID 824
Disease adrenal cortical carcinoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:11)
HP:0002664  |  Neoplasia  |  4
HP:0001635  |  Congestive heart failure  |  1
HP:0002027  |  Abdominal pain  |  1
HP:0030731  |  Carcinoma  |  1
HP:0008200  |  Primary hyperparathyroidism  |  1
HP:0001402  |  Hepatocellular carcinoma  |  1
HP:0008258  |  Congenital adrenal hyperplasia  |  1
HP:0002667  |  Wilms tumor  |  1
HP:0000843  |  Hyperparathyroidism  |  1
HP:0012531  |  Pain  |  1
HP:0008221  |  Enlarged adrenal glands  |  1
Disease ID 824
Disease adrenal cortical carcinoma
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:6)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs121912664158781427157TP53umls:C0206686BeFreeRecently, a characteristic TP53 mutation at codon 337 (R337H) has been identified in the germline of children with adrenocortical carcinoma in Southern Brazil.0.2606593772005TP53177670699CT,G,A
rs121912664160339187157TP53umls:C0206686BeFreeThe TP53 R337H mutation dramatically increases predisposition to childhood ACT but not to other cancers, and explains the increased frequency of ACT observed in this geographic region.0.2606593772006TP53177670699CT,G,A
rs121912664117534287157TP53umls:C0206686BeFreeChildren in southern Brazil that exhibit an elevated incidence of adrenocortical carcinoma (ACC) harbor an Arg 337 to His mutation within the tetramerization domain of p53 (p53-R337H; 35 of 36 patients).0.2606593772002TP53177670699CT,G,A
rs121912664126340627157TP53umls:C0206686BeFreeThe tetramerization domain for wild-type p53 (p53tet-wt) and a p53 mutant, R337H (p53tet-R337H), associated with adrenocortical carcinoma (ACC) in children, can be converted from the soluble native state to amyloid-like fibrils under certain conditions.0.2606593772003TP53177670699CT,G,A
rs28934576160965287157TP53umls:C0206686BeFreeAlthough codon 273 is a known hotspot region for p53 mutation, the patient's mutation, R273H, has not been associated with development of adrenal cortical carcinoma.0.2606593772005TP53177673802CT,A
rs387906778223154533762KCNJ5umls:C0206686BeFreeThese studies demonstrate that the T158A mutation of the KCNJ5 gene produces a marked stimulation in aldosterone biosynthesis that is dependent on membrane depolarization and sodium and calcium influx into the HAC15 adrenal cortical carcinoma cells.0.0005428842012KCNJ511128911745AG
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.)
Chemical(Total Drugs:7)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0206686aminoglutethimideD000616125-84-8adrenocortical carcinomaMESH:D018268therapeutic11572034
C0206686decitabineC0143472353-33-5adrenocortical carcinomaMESH:D018268therapeutic20231622
C0206686cisplatinD00294515663-27-1adrenocortical carcinomaMESH:D018268therapeutic11572034
C0206686mifepristoneD01573584371-65-3adrenocortical carcinomaMESH:D018268therapeutic19289534
C0206686paclitaxelD017239-adrenocortical carcinomaMESH:D018268therapeutic22156929
C0206686streptozocinD01331118883-66-4adrenocortical carcinomaMESH:D018268therapeutic11106117
C0206686vincristineD014750-adrenocortical carcinomaMESH:D018268therapeutic12015757
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)