| 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 |