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PedAM

Pediatric Disease Annotations & Medicines



   sex cord-gonadal stromal tumor
  

Disease ID 1901
Disease sex cord-gonadal stromal tumor
Definition
Neoplasms derived from the primitive sex cord or gonadal stromal cells of the embryonic GONADS. They are classified by their presumed histogenesis and differentiation. From the sex cord, there are SERTOLI CELL TUMOR and GRANULOSA CELL TUMOR; from the gonadal stroma, LEYDIG CELL TUMOR and THECOMA. These tumors may be identified in either the OVARY or the TESTIS.
Synonym
[m]specialised gonadal neoplasm nos
[m]specialised gonadal neoplasms
[m]specialized gonadal neoplasm nos
[m]specialized gonadal neoplasm nos (morphologic abnormality)
[m]specialized gonadal neoplasms
[m]specialized gonadal neoplasms (morphologic abnormality)
cord sex stromal tumors
cord sex tumors
gonadal stromal tumor
gonadal stromal tumour
sex cord stromal tumor
sex cord stromal tumour
sex cord tumor
sex cord tumor, nos
sex cord tumour
sex cord-gonadal stromal tumors
sex cord-gonadal stromal tumors [disease/finding]
sex cord-stromal neoplasm
sex cord-stromal tumor
sex cord-stromal tumor (morphologic abnormality)
sex cord-stromal tumor, no icd-o subtype
sex cord-stromal tumor, no icd-o subtype (morphologic abnormality)
sex cord-stromal tumor, no international classification of diseases for oncology subtype
sex cord-stromal tumor, no international classification of diseases for oncology subtype (morphologic abnormality)
sex cord-stromal tumors
sex cord-stromal tumour
sex cord-stromal tumour, no icd-o subtype
specialised gonadal neoplasm
specialised gonadal tumour
specialized gonadal neoplasm
specialized gonadal neoplasm (morphologic abnormality)
specialized gonadal tumor
specialized gonadal tumor (qualifier value)
tumor, sex cord-stromal
tumors, sex cord-stromal
DOID
UMLS
C0206724
MeSH
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
GNAS  |  2778  |  CLINVAR
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:177)
64132  |  XYLT2  |  DISEASES
54474  |  KRT20  |  DISEASES
7022  |  TFAP2C  |  DISEASES
6820  |  SULT2B1  |  DISEASES
2099  |  ESR1  |  DISEASES
2099  |  ESR1  |  DISEASES
7049  |  TGFBR3  |  DISEASES
1113  |  CHGA  |  DISEASES
1113  |  CHGA  |  DISEASES
57167  |  SALL4  |  DISEASES
268  |  AMH  |  DISEASES
1048  |  CEACAM5  |  DISEASES
6822  |  SULT2A1  |  DISEASES
657  |  BMPR1A  |  DISEASES
4254  |  KITLG  |  DISEASES
2026  |  ENO2  |  DISEASES
2026  |  ENO2  |  DISEASES
2956  |  MSH6  |  DISEASES
92  |  ACVR2A  |  DISEASES
652  |  BMP4  |  DISEASES
6662  |  SOX9  |  DISEASES
5300  |  PIN1  |  DISEASES
54567  |  DLL4  |  DISEASES
3852  |  KRT5  |  DISEASES
3852  |  KRT5  |  DISEASES
9210  |  BMP15  |  DISEASES
81  |  ACTN4  |  DISEASES
10468  |  FST  |  DISEASES
269  |  AMHR2  |  DISEASES
27429  |  HTRA2  |  DISEASES
5460  |  POU5F1  |  DISEASES
5460  |  POU5F1  |  DISEASES
1588  |  CYP19A1  |  DISEASES
1588  |  CYP19A1  |  DISEASES
55726  |  ASUN  |  DISEASES
10021  |  HCN4  |  DISEASES
25939  |  SAMHD1  |  DISEASES
6855  |  SYP  |  DISEASES
6855  |  SYP  |  DISEASES
90  |  ACVR1  |  DISEASES
943  |  TNFRSF8  |  DISEASES
10664  |  CTCF  |  DISEASES
658  |  BMPR1B  |  DISEASES
9759  |  HDAC4  |  DISEASES
5443  |  POMC  |  DISEASES
29999  |  FSCN3  |  DISEASES
1583  |  CYP11A1  |  DISEASES
1583  |  CYP11A1  |  DISEASES
7157  |  TP53  |  DISEASES
7157  |  TP53  |  DISEASES
84432  |  PROK1  |  DISEASES
4103  |  MAGEA4  |  DISEASES
2796  |  GNRH1  |  DISEASES
8795  |  TNFRSF10B  |  DISEASES
6770  |  STAR  |  DISEASES
6770  |  STAR  |  DISEASES
23082  |  PPRC1  |  DISEASES
23082  |  PPRC1  |  DISEASES
6768  |  ST14  |  DISEASES
3948  |  LDHC  |  DISEASES
5741  |  PTH  |  DISEASES
7345  |  UCHL1  |  DISEASES
3815  |  KIT  |  DISEASES
3815  |  KIT  |  DISEASES
54361  |  WNT4  |  DISEASES
6271  |  S100A1  |  DISEASES
1584  |  CYP11B1  |  DISEASES
3856  |  KRT8  |  DISEASES
3856  |  KRT8  |  DISEASES
3625  |  INHBB  |  DISEASES
2661  |  GDF9  |  DISEASES
143689  |  PIWIL4  |  DISEASES
5617  |  PRL  |  DISEASES
94031  |  HTRA3  |  DISEASES
1241  |  LTB4R  |  DISEASES
1241  |  LTB4R  |  DISEASES
794  |  CALB2  |  DISEASES
794  |  CALB2  |  DISEASES
7015  |  TERT  |  DISEASES
947  |  CD34  |  DISEASES
8793  |  TNFRSF10D  |  DISEASES
116028  |  RMI2  |  DISEASES
653499  |  LGALS7B  |  DISEASES
80010  |  RMI1  |  DISEASES
4684  |  NCAM1  |  DISEASES
4684  |  NCAM1  |  DISEASES
8630  |  HSD17B6  |  DISEASES
3640  |  INSL3  |  DISEASES
5745  |  PTH1R  |  DISEASES
10229  |  COQ7  |  DISEASES
23212  |  RRS1  |  DISEASES
6794  |  STK11  |  DISEASES
5241  |  PGR  |  DISEASES
5241  |  PGR  |  DISEASES
84987  |  COX14  |  DISEASES
3855  |  KRT7  |  DISEASES
3855  |  KRT7  |  DISEASES
7490  |  WT1  |  DISEASES
7490  |  WT1  |  DISEASES
4088  |  SMAD3  |  DISEASES
668  |  FOXL2  |  DISEASES
668  |  FOXL2  |  DISEASES
7270  |  TTF1  |  DISEASES
7270  |  TTF1  |  DISEASES
2626  |  GATA4  |  DISEASES
2309  |  FOXO3  |  DISEASES
93  |  ACVR2B  |  DISEASES
4089  |  SMAD4  |  DISEASES
23405  |  DICER1  |  DISEASES
23405  |  DICER1  |  DISEASES
2100  |  ESR2  |  DISEASES
2100  |  ESR2  |  DISEASES
1499  |  CTNNB1  |  DISEASES
1499  |  CTNNB1  |  DISEASES
7316  |  UBC  |  DISEASES
6146  |  RPL22  |  DISEASES
8295  |  TRRAP  |  DISEASES
5265  |  SERPINA1  |  DISEASES
284654  |  RSPO1  |  DISEASES
8794  |  TNFRSF10C  |  DISEASES
10298  |  PAK4  |  DISEASES
841  |  CASP8  |  DISEASES
5573  |  PRKAR1A  |  DISEASES
3201  |  HOXA4  |  DISEASES
6693  |  SPN  |  DISEASES
4311  |  MME  |  DISEASES
4311  |  MME  |  DISEASES
800  |  CALD1  |  DISEASES
2494  |  NR5A2  |  DISEASES
2494  |  NR5A2  |  DISEASES
7259  |  TSPYL1  |  DISEASES
5654  |  HTRA1  |  DISEASES
2018  |  EMX2  |  DISEASES
3283  |  HSD3B1  |  DISEASES
3283  |  HSD3B1  |  DISEASES
1586  |  CYP17A1  |  DISEASES
1586  |  CYP17A1  |  DISEASES
2778  |  GNAS  |  DISEASES
5728  |  PTEN  |  DISEASES
2516  |  NR5A1  |  DISEASES
2516  |  NR5A1  |  DISEASES
367  |  AR  |  DISEASES
367  |  AR  |  DISEASES
3293  |  HSD17B3  |  DISEASES
23569  |  PADI4  |  DISEASES
2159  |  F10  |  DISEASES
3963  |  LGALS7  |  DISEASES
1855  |  DVL1  |  DISEASES
190  |  NR0B1  |  DISEASES
56261  |  GPCPD1  |  DISEASES
2308  |  FOXO1  |  DISEASES
6462  |  SHBG  |  DISEASES
4267  |  CD99  |  DISEASES
4267  |  CD99  |  DISEASES
2315  |  MLANA  |  DISEASES
2315  |  MLANA  |  DISEASES
2254  |  FGF9  |  DISEASES
6736  |  SRY  |  DISEASES
6736  |  SRY  |  DISEASES
3875  |  KRT18  |  DISEASES
6370  |  CCL25  |  DISEASES
174  |  AFP  |  DISEASES
174  |  AFP  |  DISEASES
5744  |  PTHLH  |  DISEASES
2492  |  FSHR  |  DISEASES
54894  |  RNF43  |  DISEASES
7258  |  TSPY1  |  DISEASES
7258  |  TSPY1  |  DISEASES
100289087  |  TSPY10  |  DISEASES
100289087  |  TSPY10  |  DISEASES
196527  |  ANO6  |  DISEASES
196527  |  ANO6  |  DISEASES
3451  |  IFNA17  |  DISEASES
8322  |  FZD4  |  DISEASES
4090  |  SMAD5  |  DISEASES
91  |  ACVR1B  |  DISEASES
3851  |  KRT4  |  DISEASES
Locus(Waiting for update.)
Disease ID 1901
Disease sex cord-gonadal stromal tumor
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype(Waiting for update.)
Disease ID 1901
Disease sex cord-gonadal stromal tumor
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:2)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs11554273NA2778GNASumls:C0206724CLINVARNA0.12NAGNAS2058909365CA,G,T
rs121913495NA2778GNASumls:C0206724CLINVARNA0.12NAGNAS2058909366GA,T
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:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)