| UMLS CUI | UMLS Term |
Proteins |
C0001349 | Acute-Phase Reaction |
ANG |
C0001925 | Albuminuria |
ACE, AGT, GNAQ, PYCARD, IL6, INS, LEPR, MIR155, PTGS2, SOD2, TNF, CASP1 |
C0002170 | Alopecia |
PARP1, BRD4, AR, MTHFR, SRD5A2, SUPV3L1, VDR, ZFP36 |
C0002453 | Amenorrhea |
CPB2, CYP17A1, CYP19A1, FSHB, PRL |
C0002622 | Amnesia |
SIGMAR1, HRH3, GNAI1, GNAI3, APP, IL1A, IL6, NGF, POMC, PREP, TRH |
C0002624 | Retrograde Amnesia |
PREP |
C0002793 | Anaplasia |
HIF1A |
C0002938 | Aneuploidy |
KIF11 |
C0002962 | Angina Pectoris |
PLAU |
C0002965 | Angina, Unstable |
CXCL8, PAPPA, PLAU |
C0003123 | Anorexia |
IL1B, IL1RN, TNF, CCK |
C0003130 | Anoxia |
ALDH1L1, SARDH, AHCY, EGR1, GAPDH, GNAS, APOA1, ACADVL, MPO, ATF4, NME1, NOS3, PCK2, PLAT, POMC, ACTB, RPS2, RPS14, BDNF, SOD2, TFPI, TKT |
C0003537 | Aphasia |
PLAT |
C0003635 | Apraxias |
FOXP2 |
C0003811 | Cardiac Arrhythmia |
SGOL1, ACE, AGT, EDN1, ESR2, GJA1, ANK2, KCNH2, KNG1, OPRL1, CNNM2, PPP1R1A, PTGS2, TRH, CACNA1C |
C0003862 | Arthralgia |
MVK |
C0003962 | Ascites |
CHRM3 |
C0004134 | Ataxia |
EGR3, ARCN1, NPC1, SLC2A1 |
C0004238 | Atrial Fibrillation |
ACE, DES, EDN1, ESR2, SYNE2, MTHFR, ZFHX3, NOS3, NPPB, SELE, VWF, AOPEP, CAV1, CAV2 |
C0004245 | Atrioventricular Block |
GNAI2 |
C0004310 | Auditory Perceptual Disorders |
CHRNA7 |
C0004604 | Back Pain |
PLAT |
C0004610 | Bacteremia |
TIRAP, PLAT |
C0005612 | Birth Weight |
ADRB1, LCORL, LINC00908, HFE, MBL2, ENPP2, PON1, CDKAL1, HMGA2 |
C0005683 | Urinary Bladder Calculi (Disorder) |
AHR |
C0005697 | Neurogenic Urinary Bladder |
CHRM2 |
C0005699 | Blast Phase |
BCR |
C0005758 | Bulla |
ADAM17 |
C0005910 | Body Weight |
MC4R, PCSK1, POMC, CDKAL1, MAP2K5, BDNF, KLF9, FTO, SEC16B |
C0006625 | Cachexia |
CDH6, IL6, CXCL8, GHRL, PTGS2, PTHLH, TNF, ZFP36, CD27 |
C0007370 | Catalepsy |
CNR1, ADORA1, DRD2, AGT, FYN, GCG, NTS, POMC, PRL, TH, TRH, CCK |
C0007621 | Neoplastic Cell Transformation |
OCLN, AKR1C1, AKR1C2, ENO2, EPAS1, ESR1, FN1, PHGDH, SLC40A1, NRG1, APC, IGBP1, IGF1R, IL6, IL7R, CXCL8, IRS1, JUN, KRT19, LGALS3, LOXL2, MIR25, MDM2, MITF, MMP9, MUC1, MYC, MYCN, NFKB1, NOTCH1, MAPK8, RAC1, BCL2, RELA, SLC2A1, SOD2, BRCA1, ZEB1, TFRC, TGFB1, ACTG1, TNFAIP3, TP53, VIM, WHSC1, WNT5A, CXCR4, LIN28A, AKR1C3, TSC22D1, CLDN1, ZEB2 |
C0007758 | Cerebellar Ataxia |
RPL27A |
C0008489 | Chorea |
NKX2-1 |
C0008625 | Chromosome Aberrations |
CDK6, EPAS1, ERCC1, POT1, GSTM1, GSTP1, GSTT1, MYCN, XPC, XRCC4 |
C0009376 | Colonic Polyps |
ALOX5, ILK, TRPM7 |
C0009398 | Color Vision Defect |
ATF6 |
C0009421 | Comatose |
CYP2D6, GCG |
C0009806 | Constipation |
GCG, POMC, PON1 |
C0010200 | Coughing |
ACE, KNG1 |
C0010520 | Cyanosis |
ADRA2B, CYB5R3, HBB, TGFB2 |
C0010709 | Cyst |
PKD1 |
C0011053 | Deafness |
JAG1, SMAD4, MITF, POLD1, BDNF |
C0011057 | Hearing Loss, Sudden |
MTHFR |
C0011065 | Cessation Of Life |
APOA1 |
C0011071 | Sudden Death |
ACE, AGT |
C0011991 | Diarrhea |
IL1A, IL1RN, MYO5B, CD14 |
C0013362 | Dysarthria |
NPC1, PDE8B |
C0013384 | Dyskinetic Syndrome |
DRD2 |
C0013386 | Dyskinesia, Drug-Induced |
DRD2, FOSB, PENK, TH, CCK, HOMER1 |
C0013404 | Dyspnea |
NPPB |
C0013421 | Dystonia |
CYP2D6, TOR1A, CIZ1, THAP1, ACTB, SCP2, TH, PRKRA |
C0013604 | Edema |
GSR, APOA1, IL6, CXCL8, IL11, INS, KNG1, POMC, MAP2K6, PTGS2, SLC9A2, TNF, CASP8, CASP9 |
C0013608 | Edema, Cardiac |
IFT122 |
C0013911 | Emaciation |
MGME1 |
C0013990 | Pathological Accumulation Of Air In Tissues |
APOE, SERPINA1, PPP2R5A, BICD1, TP53, KL |
C0014067 | Occipital Encephalocele |
DACT1 |
C0015379 | Extravasation Of Diagnostic And Therapeutic Materials |
IL1RN, KNG1, NR1H4 |
C0015469 | Facial Paralysis |
POMC |
C0015672 | Fatigue |
TGFBR2 |
C0015799 | Feminization |
ESR1 |
C0015814 | Femur Head Necrosis |
POMC |
C0015927 | Fetal Death |
PDGFRA |
C0015934 | Fetal Growth Retardation |
COMT, AGT, LINC00908, IGF1R, IGF2, NOS3, ORC1 |
C0015951 | Fetal Resorption |
PRL |
C0015967 | Fever |
TPH2, FSHB, IL1A, IL1B, IL6, CXCL8, MVK, POMC, PRL, SOD2, TNF |
C0016059 | Fibrosis |
ATP6AP2, COL1A1, COL1A2, COL3A1, ADRB2, CYP19A1, DCN, AGT, AKT1, ALB, ANGPT1, HMOX1, IL1B, IL1RN, LEPR, MIR21, PDGFB, PIK3CG, MAP2K7, PTGS2, SOD2, STAT3, TGFB1, THBS1, TNF, PDGFD, SPHK1, CCND2 |
C0016382 | Flushing |
ALDH2, PTGS1 |
C0017639 | Gliosis |
FGF2, TNFRSF21, GRM8, ITGA2, ITGA5, ITGB1, ITGB3, ITGB4, KCNK3, MAPK1, MAPK3, BDNF, TNR |
C0018128 | Graft Occlusion, Vascular |
PLAU |
C0018199 | Granuloma, Plasma Cell |
RANBP2 |
C0018200 | Granuloma, Respiratory Tract |
SOD2 |
C0018273 | Growth Disorders |
PQBP1, CNTN4, AHR, GH1, AFF4, SH3PXD2B, HMOX1, IGF1R, IGF2, LTBP3, MIR17HG, PIK3CA, ATRX, AVPR2, PTHLH, BUB1B, SECISBP2 |
C0018524 | Hallucinations |
HOMER1 |
C0018681 | Headache |
GNRH1, IL6 |
C0018781 | Noise-Induced Hearing Loss |
TAOK1 |
C0018784 | Sensorineural Hearing Loss (Disorder) |
COL9A1, COL11A2, LRP2, ACTB, FADD |
C0018794 | Heart Block |
LMNA |
C0018800 | Cardiomegaly |
CPT1B, ADRA1B, CTF1, CYP1A1, CYP1B1, CYP2E1, DMD, AGT, EDN1, AHR, AKT1, FGF2, CABIN1, GAS6, GATA4, GSK3B, HDAC2, HIF1A, HMOX1, HTR2B, IGF1, IL1B, IL18, ITPR2, LIF, MIR21, MT2A, NOS3, NPPB, ATP2A2, PIK3CG, PLD1, POMC, PPARA, PPARD, PRKAA2, PRKCA, PRKCB, RRAD, SOD2, STAT3, TNF, TRPC1, UCP2, CAV1, CCND2, MFN2 |
C0018834 | Heartburn |
TRPV1 |
C0018944 | Hematoma |
S100B |
C0018946 | Hematoma, Subdural |
PLAT |
C0018965 | Hematuria |
PLAU, POMC |
C0018991 | Hemiplegia |
CGA |
C0019054 | Hemolysis (Disorder) |
G6PD, SLC40A1, HMOX1, HP |
C0019080 | Hemorrhage |
CYP2C9, F2, FOS, IL11, ITGB3, SERPINA1, PLAT, PLAU, POMC, VKORC1 |
C0019209 | Hepatomegaly |
LEPR, TRIM37, PPARA |
C0019284 | Diaphragmatic Hernia |
CFTR, AGT, EDN1, EDNRA, FGF2, ZFPM2, GATA4, GATA6, GJA1, ICAM1, IGF1, IGF2, IL6, KCNMA1, LRP2, NOS3, SFTPC, BMP4, NR2F2, TGFB1, THRA, NKX2-1, TNF, UCHL1, VCAM1, WT1, FGF18 |
C0019294 | Hernia, Inguinal |
TGFBR2 |
C0019572 | Hirsutism |
POMC, CACNA1G |
C0020305 | Hydrops Fetalis |
CCBE1 |
C0020429 | Hyperalgesia |
CNR1, ADM, CSK, AGT, EDN1, ALOX5, IGF1, IL1A, IL1B, IL1RN, IL6, CXCL8, IL10, INSR, ITGA2, KNG1, NGF, TNFRSF11B, GAL, MAPK1, MAPK3, MAPK7, PTGS1, PTGS2, PTHLH, RAF1, TRPV4, CCL2, SPARC, SYN2, TNF, TRPV1, CACNA2D1, CCKBR, CARTPT |
C0020433 | Hyperbilirubinemia |
TNF |
C0020438 | Hypercalciuria |
POMC, PTH |
C0020455 | Hypergammaglobulinemia |
B2M |
C0020505 | Hyperphagia |
LEP, LEPR, MC4R, NTRK2 |
C0020507 | Hyperplasia |
PRG4, AKT1, KDM1A, BRD4, HIF1A, HMOX1, HSPB1, KCNK1, LDLR, MMP9, MYCN, PIK3CA, PTGS2, TCF7L2, TGFB1, ZFP36 |
C0020578 | Hyperventilation |
VAV3, AHR |
C0020672 | Hypothermia, Natural |
CNR1, GCG, GNRH1, IL12A, LHB, TNF, TRH |
C0020796 | Profound Mental Retardation |
MTR |