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
|