UMLS CUI |
UMLS Term |
Proteins |
C0041327
|
Tuberculosis, Pulmonary
|
CD209,
ASAP1,
CCL2
|
C0041341
|
Tuberous Sclerosis
|
TSC2
|
C0041408
|
Turner Syndrome
|
GH1,
SOD2
|
C0041409
|
Turner Syndrome, Male
|
PTPN11
|
C0041466
|
Typhoid Fever
|
HLA-DRB1
|
C0041582
|
Ulcer
|
PPIF,
DDIT3
|
C0041657
|
Unconscious State
|
TRH,
CCK
|
C0041755
|
Adverse Reaction To Drug
|
ABCC4,
PLK2,
CLU,
ADORA1,
COMMD1,
CYP2C9,
CYP2D6,
CYP2E1,
DHFR,
ALB,
FGA,
HLA-B,
HLA-C,
HMOX1,
HTR2B,
IGF1,
IGFBP1,
KITLG,
ABCC1,
MTHFR,
MTR,
PPARA,
PTGS2,
SHMT1,
SLC19A1,
SLCO2A1,
SPP1,
TOP1,
TYMS,
ARID5B,
HOMER1
|
C0041834
|
Erythema
|
ACSL4
|
C0041948
|
Uremia
|
ICAM1,
MGP,
NOS3,
TNFRSF11B,
PTH,
BMP2,
SPARC,
SPP1,
TGFB1,
TGFBR1,
VCAM1,
VDR,
RUNX2
|
C0041955
|
Ureteral Neoplasms
|
AHR
|
C0041956
|
Ureteral Obstruction
|
COL3A1,
TGFB1,
TGFB2
|
C0042029
|
Urinary Tract Infection
|
POMC
|
C0042035
|
Urination Disorders
|
TRPV4
|
C0042063
|
Urogenital Abnormalities
|
TGFB2
|
C0042065
|
Genitourinary Neoplasms
|
TP53
|
C0042076
|
Urologic Neoplasms
|
FHIT,
TP53
|
C0042109
|
Urticaria
|
ALB,
ALOX5,
GSTM1,
HLA-DQB1,
HLA-DRB1,
HNMT,
ICAM1,
IL1B,
IL18,
MPO,
SELE,
TGFB1,
TNF,
VCAM1
|
C0042131
|
Uterine Diseases
|
CGA
|
C0042133
|
Uterine Fibroids
|
TNRC6B,
BET1L
|
C0042138
|
Uterine Neoplasms
|
CDKN1B,
HMGA1,
INHBA,
KRAS,
SMAD3
|
C0042164
|
Uveitis
|
ALB,
SERPINF1,
SOD2,
CALB2
|
C0042345
|
Varicosity
|
TNC,
MGP,
TIMP1
|
C0042373
|
Vascular Diseases
|
MYL9,
AHR,
ALDH2,
GCG,
HGF,
MTHFR,
MYLK,
PKD2,
SOD2,
TIMP1,
TNF,
VKORC1
|
C0042384
|
Vasculitis
|
SERPINA1
|
C0042487
|
Venous Thrombosis
|
F2,
F5,
F8,
F13A1,
F13B,
JAK2,
MTHFR,
SERPINC1,
PLAT,
PLAU,
PLG,
TFPI
|
C0042510
|
Ventricular Fibrillation
|
DSP,
INS,
PLAU
|
C0042512
|
Ventricular Outflow Obstruction
|
INS
|
C0042514
|
Tachycardia, Ventricular
|
LMNA,
NOS3,
NPPB,
RYR2
|
C0042594
|
Vestibular Diseases
|
GSTP1,
GSTZ1,
NOS3
|
C0042769
|
Virus Diseases
|
IFNAR1
|
C0042781
|
Visceral Myopathy
|
ACTG2
|
C0042790
|
Vision Disorders
|
CLN6
|
C0042842
|
Vitamin A Deficiency
|
PARP1,
RBP4,
BMP4
|
C0042847
|
Vitamin B 12 Deficiency
|
ABCD4
|
C0042870
|
Vitamin D Deficiency
|
CYP2R1,
GC,
LRP2,
NADSYN1,
VDR
|
C0042900
|
Vitiligo
|
SH2B3,
TOB2,
PTPN22,
FOXP1,
LPP,
RERE,
ZMIZ1,
BACH2,
SMOC2,
IKZF4,
SLC1A2,
TYR,
RNASET2,
CD44
|
C0042963
|
Vomiting
|
GNRH1
|
C0042974
|
Von Willebrand Disease
|
VWF
|
C0043019
|
Lateral Medullary Syndrome
|
FSHB
|
C0043020
|
Wallerian Degeneration
|
CCAR2
|
C0043094
|
Weight Gain
|
FSTL1,
AKAP2,
OSBPL8,
CNR1,
NEK7,
CTSD,
CYP2D6,
DYNC1LI2,
DRD2,
FBLN2,
MAPRE1,
PALLD,
MPRIP,
GH1,
GNB3,
PTRF,
FAM126B,
GRB14,
ANXA2,
ANXA5,
APBB2,
HTR2C,
IGFBP5,
APP,
LEP,
STS,
MEST,
MYO10,
NID1,
NPR3,
SEPSECS,
ZDHHC2,
PCYOX1,
GHRL,
PIK3CA,
POMC,
PPARD,
ZWILCH,
NDC1,
PRPS1,
STIM2,
BCAT1,
RFNG,
RPL28,
RPS8,
SPARC,
SPTBN1,
TNF,
TPM4,
VIM,
SORBS2,
CAV1,
DNAH11,
IQGAP1,
LARGE,
ADIPOQ,
CD36,
GDF15,
LPGAT1
|
C0043119
|
Werner Syndrome
|
LMNA
|
C0043121
|
Wernicke Encephalopathy
|
TKT
|
C0043207
|
Wolfram Syndrome
|
CISD2
|
C0043208
|
Wolman Disease
|
LIPA
|
C0043346
|
Xeroderma Pigmentosum
|
POLH,
XPA
|
C0043459
|
Zellweger Syndrome
|
HSD17B4,
PEX12,
PEX14,
ABCD3,
PEX3,
PEX11B
|
C0078918
|
Albinism, Oculocutaneous
|
MITF,
TYR
|
C0079153
|
Hyperkeratosis, Epidermolytic
|
ERCC2,
KRT1
|
C0079218
|
Fibromatosis, Aggressive
|
APC,
TNF
|
C0079294
|
Epidermolysis Bullosa Dystrophica
|
MMP1
|
C0079298
|
Epidermolysis Bullosa Simplex
|
ITGB4
|
C0079301
|
Junctional Epidermolysis Bullosa
|
ITGB4,
LAMA3
|
C0079474
|
Hallopeau-Siemens Disease
|
MMP1
|
C0079487
|
Helicobacter Infections
|
CDKN1B,
IFNGR1,
TFRC
|
C0079541
|
Holoprosencephaly
|
GAS1,
PTCH1,
TDGF1
|
C0079588
|
Ichthyosis, X-Linked
|
STS
|
C0079683
|
Herlitz Disease
|
LAMA3
|
C0079731
|
B-Cell Lymphomas
|
NRAS,
PTGS2
|
C0079744
|
Diffuse Large B-Cell Lymphoma
|
PRDX4,
TXNIP,
EZH2,
SEC31A,
HLA-B,
FAS,
PIK3CA,
PIK3CB,
PIK3CD,
PIK3CG,
B2M,
PVT1,
BCL2,
ARAP3,
NOM1,
SKP2,
SOD2,
SOD3,
CDK1
|
C0079770
|
Lymphoma, Small Noncleaved-Cell
|
MYC
|
C0079772
|
T-Cell Lymphoma
|
DDX3X,
EP300,
MGA,
RHOA,
PPARG,
BCL6,
STAT3,
STAT5B,
TP53,
ARID1A
|
C0079773
|
Lymphoma, T-Cell, Cutaneous
|
FAS,
RHOA,
MCL1,
PRKCQ,
BAX,
STAT5B,
ZEB1,
TNFAIP3,
TP53,
ARID1A,
CD28
|
C0079774
|
Peripheral T-Cell Lymphoma
|
FYN,
IDH2,
RHOA,
B2M,
CD28,
CD58
|
C0079840
|
Milk Hypersensitivity
|
FAM117A
|
C0080024
|
Piebaldism
|
KIT,
SNAI2
|
C0080178
|
Spina Bifida
|
CFL1,
CHKA,
FGFR2,
TXN2,
PCMT1,
PCYT1A,
PDGFRA,
PON1,
CCL2
|
C0080274
|
Urinary Retention
|
EDN1
|
C0080333
|
Weber-Cockayne Syndrome
|
ITGB4
|
C0085083
|
Ovarian Hyperstimulation Syndrome
|
FSHR
|
C0085084
|
Motor Neuron Disease
|
VIM
|
C0085096
|
Peripheral Vascular Diseases
|
CYP1A1
|
C0085106
|
Familial Benign Pemphigus
|
ATP2C1
|
C0085109
|
Corneal Neovascularization
|
FGF2,
VEGFA
|
C0085110
|
Severe Combined Immunodeficiency
|
ADA,
IL7R,
JAK3,
RAG1,
DCLRE1C,
TFRC
|
C0085128
|
Cardiac Output, High
|
NPPB
|
C0085129
|
Bronchial Hyperreactivity
|
SPON2,
CXCL1,
ICAM1,
IL1RN,
NGF,
PTGS1,
CCL2
|
C0085136
|
Central Nervous System Neoplasms
|
TP53
|
C0085179
|
Eosinophilia-Myalgia Syndrome
|
HLA-DQA1,
HLA-DRB1
|
C0085183
|
Neoplasms, Second Primary
|
DAPK1,
GSTM1,
RAD9A
|
C0085207
|
Gestational Diabetes
|
IGF2BP2,
CYP19A1,
FGF2,
AR,
LEP,
LEPR,
MBL2,
CDKAL1,
SOD2,
ADIPOQ
|
C0085215
|
Ovarian Failure, Premature
|
FMR1,
WT1
|
C0085220
|
Cerebral Amyloid Angiopathy
|
APOE,
APP
|
C0085261
|
Proteus Syndrome
|
AKT1,
PTEN
|
C0085280
|
Alagille Syndrome
|
JAG1,
NOTCH2
|
C0085298
|
Sudden Cardiac Death
|
DSP,
KCNH2,
LMNA,
TMEM43
|
C0085307
|
Embolism And Thrombosis
|
PLAT
|
C0085390
|
Li-Fraumeni Syndrome
|
MDM2,
TP53
|
C0085397
|
Pasteurellaceae Infections
|
CRP,
HP
|
C0085413
|
Polycystic Kidney, Autosomal Dominant
|
BRD4,
MYC,
PKD1,
PKD2,
PPARG
|
C0085548
|
Autosomal Recessive Polycystic Kidney Disease
|
EGFR,
NPHP3
|
C0085568
|
Buruli Ulcer
|
SLC11A1
|
C0085602
|
Polydipsia
|
LEP
|
C0085605
|
Liver Failure
|
F2,
ORM1,
VEGFA
|
C0085628
|
Stupor
|
TRH
|
C0085636
|
Photophobia
|
ATF6
|
C0085655
|
Polymyositis
|
CYP27B1,
IL1A,
IL1B,
IL6,
TNF
|
C0085681
|
Hyperphosphatemia (Disorder)
|
PTH,
KL
|
C0086132
|
Depressive Symptoms
|
PARVA
|