C0036421
|
Systemic Scleroderma
|
JAZF1,
ANKS1A,
TNPO3,
GRB10,
HLA-DPA1,
HLA-DQB1,
HLA-DRA,
ITGAM,
RHOB,
PXK,
KIAA0319L
|
C0036429
|
Sclerosis
|
IL1RN
|
C0036439
|
Scoliosis, Unspecified
|
NOTCH1
|
C0036457
|
Scrapie
|
ATF6,
PRNP
|
C0036489
|
Sea-Blue Histiocyte Syndrome
|
APOE
|
C0036572
|
Seizures
|
SIGMAR1,
CHRNA5,
CHRNA7,
CLU,
CNR1,
ADRA1B,
CYP11A1,
ABAT,
DRD2,
AGT,
ALAD,
FGF2,
FOXG1,
FOS,
ALPL,
GABRA5,
GNB3,
APOE,
IL1B,
IL6,
IMPA1,
INS,
KCNJ11,
LEP,
LETM1,
MT3,
NGF,
NGFR,
PAM,
GHRL,
POLG,
POMC,
RBFOX1,
CNNM2,
PRKCD,
PTGS2,
MIB1,
BDNF,
SLC2A1,
SLC6A1,
SOD2,
SYN2,
TCF4,
TRH,
TSC2,
SLC30A1,
NRP2,
CCK
|
C0036631
|
Seminoma
|
ENTPD6
|
C0036830
|
Serum Sickness
|
ALB
|
C0036875
|
Disorders Of Sex Development
|
AKR1C1,
AKR1C2,
LHCGR,
AKR1C3
|
C0036920
|
Sezary Syndrome
|
CDKN1B,
CREBBP,
MAPK1,
PTEN,
KMT2C,
RB1,
RPS6KA1,
SMARCA4,
ZEB1,
TNFRSF1B,
TP53,
ARID1A,
BCL10,
IL32
|
C0036980
|
Shock, Cardiogenic
|
PLAT,
SOD2
|
C0036982
|
Shock, Hemorrhagic
|
CXCL1,
CXCL2,
ICAM1,
IL6,
MPO,
TNF
|
C0036983
|
Septic Shock
|
GC,
TNF,
C5AR1
|
C0036996
|
Short Rib-Polydactyly Syndrome
|
NEK1
|
C0037019
|
Shy-Drager Syndrome
|
COQ2
|
C0037052
|
Sick Sinus Syndrome
|
POMC
|
C0037116
|
Silicosis
|
AHR,
IL1B,
CCL2
|
C0037188
|
Sinoatrial Block
|
LMNA
|
C0037198
|
Sinus Thrombosis, Intracranial
|
F2,
MTHFR
|
C0037199
|
Sinusitis
|
CFTR,
MET,
AZGP1
|
C0037221
|
Situs Inversus
|
ACVR2B
|
C0037231
|
Sjogren-Larsson Syndrome
|
ALDH3A2
|
C0037268
|
Skin Abnormalities
|
ERCC2,
FGFR2,
IRF6,
SOD2,
SUPV3L1
|
C0037274
|
Dermatologic Disorders
|
N4BP2L2,
ERCC2,
FGFR2,
RUFY3,
TNIK,
GOLGA4,
CXCL2,
GSTM1,
TRA2A,
HSPA1B,
ID2,
IL1A,
IL1B,
IL1R1,
IL1RN,
IL6,
MTHFR,
GADD45B,
NDUFB8,
NR4A2,
PFKFB3,
ZFAND6,
ZNF331,
MMP26,
PELI1,
PTEN,
PTGS2,
PTX3,
CCL4,
CCL20,
SFPQ,
SKIL,
SOD2,
SSBP1,
TRAPPC10,
TNF,
TNFAIP6,
UBE2E1,
TAF1D,
IER3,
USP13,
CD83,
KL,
GSTO1,
MINPP1,
CD44
|
C0037286
|
Skin Neoplasms
|
ERBB4,
ERCC2,
AKT1,
POT1,
GJA1,
GLI2,
GYPA,
HIF1A,
IGF1R,
IL1A,
AQP3,
KRT1,
KRT17,
MMP9,
ODC1,
PPARD,
PTCH1,
PTGS2,
RELA,
SOD2,
TGFB1,
TGFBR1,
TP53,
TYR,
XPA,
CASP8
|
C0037299
|
Skin Ulcer
|
ITGB2,
LAMA3,
NGF
|
C0037316
|
Sleep Deprivation
|
PTGS1
|
C0037579
|
Soft Tissue Neoplasms
|
BCL2,
TNF
|
C0037763
|
Spasm
|
GCG
|
C0037769
|
West Syndrome
|
SIK1,
PLCB1,
HSD17B4,
PIGA,
POMC,
ST3GAL3,
TSC2
|
C0037771
|
Paraparesis, Spastic
|
TECPR2
|
C0037772
|
Spastic Paraplegia
|
CYP2U1
|
C0037773
|
Spastic Paraplegia, Hereditary
|
PQBP1,
TECPR2,
MFN2
|
C0037822
|
Speech Disorders
|
GRIN2A,
MFSD2A
|
C0037889
|
Hereditary Spherocytosis
|
DHODH,
UMPS,
CAD
|
C0037917
|
Spina Bifida Cystica
|
CHRNA7
|
C0037926
|
Compression Of Spinal Cord
|
PLAT,
CCL2,
TNF
|
C0037928
|
Spinal Cord Diseases
|
ADA,
APP,
MTHFR
|
C0037932
|
Curvature Of Spine
|
IFT122
|
C0037997
|
Splenic Diseases
|
AHR
|
C0038002
|
Splenomegaly
|
OCLN,
AHR,
APOE,
NOTCH1
|
C0038013
|
Ankylosing Spondylitis
|
MICA,
ANTXR2,
ANO6,
HLA-A,
HLA-B,
ERAP1,
PTGER4,
IL1R2,
RUNX3
|
C0038160
|
Staphylococcal Infections
|
ACE,
CXCL8,
TLR2,
CD36
|
C0038220
|
Status Epilepticus
|
CDH2,
CNR1,
DMD,
EIF2S1,
FOS,
GAP43,
ANK3,
HMOX1,
HSPB1,
IL1RN,
JUN,
JUNB,
JUND,
KCNMA1,
LAMP2,
MEF2C,
NGF,
ATP2A2,
NTRK2,
PTGS2,
BDNF,
CCL2,
CCL3,
SNTA1,
SSTR1,
SSTR5,
TNF,
VEGFA,
CASP1,
CASP8,
PDXK
|
C0038273
|
Stereotypic Movement Disorder
|
MEF2C,
TRH
|
C0038325
|
Stevens-Johnson Syndrome
|
IKZF1,
CELF2,
PARP1,
CTNNB1,
EP300,
ALB,
HLA-A,
HLA-B,
HLA-C,
MIF,
NUCB1,
PTGER3,
PTGIS,
RB1,
VCP,
CUL4A,
CAV1,
ELMO1,
RBX1
|
C0038354
|
Stomach Diseases
|
GCG,
ANXA1
|
C0038356
|
Stomach Neoplasms
|
CDH2,
CDK4,
CDKN1A,
CDKN1B,
CNPY2,
DLC1,
FST,
NOP56,
ARL6IP5,
CCT7,
CTSC,
WIF1,
CKB,
CLCN3,
CLN3,
PLIN2,
DCBLD2,
KLF6,
CLDN3,
CTNNA2,
CTSL,
ADRB1,
ADRB2,
CYP2A6,
ACE,
GADD45A,
DES,
DNMT1,
DNMT3B,
DPYD,
HBEGF,
AGTR2,
TYMP,
ECHS1,
EEF1A1,
EEF1A2,
EGFR,
AHR,
ENO1,
ERBB2,
ERCC1,
ERCC2,
ALB,
F2R,
ALDH1A3,
FBP1,
FGFR2,
FGG,
FHIT,
FKBP2,
FAM168A,
BOP1,
ALOX5,
FYN,
SERBP1,
ZBTB20,
GREM1,
SNX5,
PRPF19,
GLI3,
MRPS18B,
PYCARD,
GSTP1,
CPSF1,
ANXA5,
ZNRD1,
HMOX1,
HNRNPL,
HOXA2,
APC,
HSPB1,
BIRC5,
HSPD1,
APOA1,
ID4,
IDH3B,
IGFBP3,
IGFBP7,
IL1B,
IL1RN,
IL6,
IL6R,
CXCL8,
IRF1,
ITGA5,
JUN,
AREG,
KISS1,
KRAS,
KRT8,
RHOA,
LGALS3,
FADS1,
SMAD4,
MARK1,
MET,
MMP10,
MT2A,
MTHFR,
MUC1,
MUTYH,
MYC,
NDUFA2,
NDUFS1,
NOS3,
NPM1,
NT5E,
ALDH7A1,
PA2G4,
SERPINE1,
ZNF593,
C11orf73,
PDHA1,
POLR3K,
PGAM1,
PHB,
SERPINA1,
PIK3CA,
PLAGL1,
PLAU,
PPARG,
XAF1,
PPIA,
PPIC,
PPP2R1A,
PPP2R4,
PREP,
CARKD,
PRKCB,
MAPK1,
MAPK3,
MAPK8,
PRNP,
KLK10,
PTGS2,
RANBP10,
PTPRF,
PTPRG,
KMT2C,
RAD23A,
RARRES1,
RBP1,
RBP4,
RGS2,
RORA,
RPL13,
RPL15,
RPL18,
RPS6,
RPS21,
RPS26,
RXRB,
BDNF,
BID,
BLVRB,
BMP2,
SLC1A2,
SNRPB,
BNIP3,
SOD2,
SREBF2,
STAT3,
ACTC1,
TGFA,
TIMP3,
TNF,
TP53,
TPM3,
TWIST1,
TYMS,
UMPS,
CA2,
ULBP2,
TAF15,
SYMPK,
ARID1A,
CASP8,
ARFGAP2,
ZNF559,
KISS1R,
CAV1,
PLPP1,
RUNX3,
AKR1C3,
IRS2,
SUCLG1,
SELENBP1,
ZNF160,
AURKB,
IL32,
CD44,
TMEM63A,
MTSS1
|
C0038358
|
Gastric Ulcer
|
ADM,
NRG1,
IAPP,
IL1B,
LEP,
MMP9,
NOS3,
GHRL,
PTGS1,
PTGS2,
TNF,
VEGFA,
CCK
|
C0038362
|
Stomatitis
|
NBN
|
C0038368
|
Stomatognathic Diseases
|
FADD
|
C0038379
|
Strabismus
|
SPG20
|
C0038436
|
Post-Traumatic Stress Disorder
|
PRTFDC1,
LGR6
|
C0038454
|
Cerebrovascular Accident
|
ACE,
EDN1,
ALB,
F2,
F5,
ALDH2,
APOA1,
ICAM1,
IL1B,
IL1RN,
IL6,
IRF1,
ITGAV,
ITGB3,
MTHFR,
ZFHX3,
PDE4D,
PLAT,
PLAU,
PRKAA2,
PTGS2,
TGFB1,
TNF,
TWIST1,
UCP2,
VKORC1,
PLA2G7,
HDAC9
|
C0038505
|
Sturge-Weber Syndrome
|
GNAQ,
RASA1
|
C0038525
|
Subarachnoid Hemorrhage
|
ADORA1,
EDN1
|
C0038580
|
Substance Dependence
|
SH3BP5
|
C0038587
|
Substance Withdrawal Syndrome
|
ARL6IP5,
CHRNA5,
CHRNA7,
CNR1,
ADORA1,
CREB1,
CRP,
DRD2,
FOS,
GNAI1,
GNAS,
GRIN2A,
HRH1,
HTR2C,
MMP9,
NPTX2,
NPY2R,
OPRL1,
PER1,
POMC,
MAPK1,
MAPK3,
PRL,
BDNF,
SLC6A1,
CCKBR
|
C0038644
|
Sudden Infant Death Syndrome
|
CHRNA7,
KCNH2
|
C0038814
|
Sunburn
|
ERCC2,
TYR
|
C0038833
|
Superior Vena Cava Syndrome
|
PTHLH
|
C0038868
|
Progressive Supranuclear Palsy
|
STX6,
MAPT
|
C0039075
|
Syndactyly
|
FZD4
|
C0039101
|
Synovial Sarcoma
|
BCL2,
VIM
|
C0039103
|
Synovitis
|
HLA-B,
POMC
|
C0039231
|
Tachycardia
|
VAV3,
DRD2,
AHR,
GCG,
GNAS,
GNRH1,
INS,
LEP,
LHB,
GAL,
RYR2,
SCT,
TNF,
TRH
|
C0039239
|
Sinus Tachycardia
|
GCG
|
C0039263
|
Takayasu Arteritis
|
HLA-B,
MLX
|
C0039292
|
Tangier Disease
|
ABCA1
|
C0039338
|
Taste Disorders
|
FAS
|
C0039373
|
Tay-Sachs Disease
|
GM2A,
HEXA
|
C0039445
|
Hereditary Hemorrhagic Telangiectasia
|
SMAD4
|
C0039483
|
Giant Cell Arteritis
|
PTPN22
|
C0039584
|
Testicular Diseases
|
TSC22D3,
PPP3CA
|
C0039585
|
Androgen-Insensitivity Syndrome
|
AR
|
C0039590
|
Testicular Neoplasms
|
ERCC1,
ERCC4,
KITLG,
ATF7IP
|
C0039621
|
Tetany
|
CNNM2
|
C0039685
|
Tetralogy Of Fallot
|
CITED2,
JAG1,
FOXC1,
ZFPM2,
GATA4,
GATA6,
GJA5,
TBX1,
NRP1
|
C0039841
|
Thiamine Deficiency
|
SERPINA1
|
C0039978
|
Thoracic Diseases
|
ATRX
|
C0039981
|
Thoracic Neoplasms
|
SMARCA4
|
C0040015
|
Thrombasthenia
|
ITGB3
|
C0040028
|
Thrombocythemia, Essential
|
SH2B3,
FGF2,
JAK2,
PDGFA,
PDGFB,
TGFB1,
TP53,
CALR
|
C0040034
|
Thrombocytopenia
|
ALB,
FCGR2A,
GP1BB,
HLA-A,
ITGB3,
MTHFR,
PECAM1,
PF4,
CYCS,
XDH,
WDR1
|
C0040038
|
Thromboembolism
|
MERTK,
F2,
F5,
GAS6,
JAK2,
PLAT,
PLAU
|
C0040053
|
Thrombosis
|
MERTK,
CRP,
CYP3A5,
AGT,
F2,
F5,
FCGR2A,
FGA,
FUT4,
GAS6,
HGF,
HMOX1,
SERPINC1,
SERPINE1,
PDE3A,
PF4,
PLAT,
PLAU,
PTGER3,
PTGS2,
TNF,
TYRO3,
VWF
|
C0040100
|
Thymoma
|
CYLD,
PBRM1,
TP53,
BAP1
|
C0040128
|
Thyroid Diseases
|
CNST,
DIO2,
ID2,
ID3,
ITGB5,
CCL2,
KLF9
|
C0040136
|
Thyroid Neoplasm
|
EPOR,
HIF1A,
HPGD,
IL1B,
IL6,
CXCL8,
KRAS,
PDGFA,
ENPP2,
PPARG,
PTGS2,
CCL2,
SLC5A5,
TNF,
TP53,
TPM3,
TPR,
PRDM2,
NCOA4,
TCF7L1
|
C0040156
|
Thyrotoxicosis
|
MTHFR
|
C0040336
|
Tobacco Use Disorder
|
CHRNA5,
CHRNA7,
CYP2A6,
DRD2,
AHR,
LCP1,
BDNF
|
C0040411
|
Tongue Neoplasms
|
CRYAB,
HSPB1,
AQP3,
PTGS2,
SOD2,
TYMS
|
C0040427
|
Tooth Abnormalities
|
FGFR2,
PITX2,
TMCO1,
ANKH,
RUNX2
|
C0040460
|
Toothache
|
NPY1R
|
C0040479
|
Torsades De Pointes
|
CYP3A4,
ANK2,
KCNH2
|
C0040588
|
Tracheoesophageal Fistula
|
PCSK5
|
C0040822
|
Tremor
|
ADRB2,
CYP2D6,
TRH
|
C0040954
|
Infection By Trichuris Trichiura
|
MPO
|
C0041207
|
Truncus Arteriosus, Persistent
|
SEMA3C,
GATA6
|
C0041296
|
Tuberculosis
|
CORO1A,
TIRAP,
STXBP5,
C2CD2,
HP,
ASAP1,
SLC11A1
|