class name | count |
---|---|
eudicotyledons | 5 |
class name | count |
---|---|
Papaveraceae | 5 |
br08003 Category | # of metabolite |
---|---|
Isoquinoline alkaloids | 3 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Isoquinoline alkaloids | C06174 | C00001837 |
Isoquinoline alkaloids | C01516 | C00001889 |
Isoquinoline alkaloids | C06171 | C00027603 |
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
---|---|---|---|---|---|---|
C00001837
![]() |
Codeine
/ (-)-Codeine |
CHEMBL485
CHEMBL22662 CHEMBL612012 CHEMBL1907378 |
D003061
|
16 / 12 / 6 | 6 / 66 |
![]() |
C00001889
![]() |
Morphine
/ (-)-Morphine |
CHEMBL70
CHEMBL1888905 CHEMBL2133708 CHEMBL2139208 |
D009020
|
32 / 17 / 11 | 71 / 199 |
![]() |
C00027603
![]() |
6-Oxocodeine
/ (-)-Codeinone |
CHEMBL163490
CHEMBL257627 |
C046414
|
1 / 0 / 0 | 5 / 2 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P35372 | Mu-type opioid receptor | Opioid receptor | C00001837 C00001889 C00027603 | 0 / 0 |
P16662 | UDP-glucuronosyltransferase 2B7 | Enzyme | C00001837 C00001889 | 0 / 0 |
Q9HAW8 | UDP-glucuronosyltransferase 1-10 | Enzyme | C00001837 C00001889 | 0 / 0 |
Q12809 | Potassium voltage-gated channel subfamily H member 2 | KCNH, Kv10-12.x (Ether-a-go-go) | C00001837 C00001889 | 2 / 2 |
O15245 | Solute carrier family 22 member 1 | Drug uniporter | C00001837 C00001889 | 0 / 0 |
P35498 | Sodium channel protein type 1 subunit alpha | SCN alpha, NaV1.x | C00001837 C00001889 | 3 / 2 |
P08183 | Multidrug resistance protein 1 | drug | C00001837 C00001889 | 1 / 0 |
Q99250 | Sodium channel protein type 2 subunit alpha | SCN alpha, NaV1.x | C00001837 C00001889 | 2 / 2 |
P22310 | UDP-glucuronosyltransferase 1-4 | Enzyme | C00001837 C00001889 | 3 / 0 |
P41145 | Kappa-type opioid receptor | Opioid receptor | C00001837 C00001889 | 0 / 0 |
Q9NY46 | Sodium channel protein type 3 subunit alpha | SCN alpha, NaV1.x | C00001837 C00001889 | 0 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001837 C00001889 | 1 / 0 |
P54855 | UDP-glucuronosyltransferase 2B15 | Enzyme | C00001837 C00001889 | 0 / 0 |
P06133 | UDP-glucuronosyltransferase 2B4 | Enzyme | C00001837 C00001889 | 0 / 0 |
P41143 | Delta-type opioid receptor | Opioid receptor | C00001837 C00001889 | 0 / 0 |
Q9HAW9 | UDP-glucuronosyltransferase 1-8 | Enzyme | C00001837 C00001889 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00001889 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001889 | 0 / 0 |
Q99720 | Sigma non-opioid intracellular receptor 1 | Membrane receptor | C00001889 | 1 / 0 |
Q9Y4X1 | UDP-glucuronosyltransferase 2A1 | Enzyme | C00001889 | 0 / 0 |
P08913 | Alpha-2A adrenergic receptor | Adrenergic receptor | C00001889 | 0 / 0 |
P36537 | UDP-glucuronosyltransferase 2B10 | Enzyme | C00001889 | 0 / 0 |
O60656 | UDP-glucuronosyltransferase 1-9 | Enzyme | C00001889 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001889 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001889 | 0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00001889 | 0 / 0 |
P22309 | UDP-glucuronosyltransferase 1-1 | Enzyme | C00001889 | 5 / 1 |
P19224 | UDP-glucuronosyltransferase 1-6 | Enzyme | C00001889 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00001889 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001889 | 0 / 1 |
P21397 | Amine oxidase [flavin-containing] A | Oxidoreductase | C00001889 | 1 / 1 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00001889 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
581 | BAX, BCL2L4 | BCL2-associated X protein |
C00001889
C00027603
|
596 | BCL2, Bcl-2, PPP1R50 | B-cell CLL/lymphoma 2 |
C00001889
C00027603
|
836 | CASP3, CPP32, CPP32B, SCA-1 | caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) |
C00001889
C00027603
|
842 | CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 | caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) |
C00001889
C00027603
|
54205 | CYCS, CYC, HCS, THC4 | cytochrome c, somatic |
C00001889
C00027603
|
1565 | CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 | cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) |
C00001837
C00001889
|
6352 | CCL5, D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228, eoCP | chemokine (C-C motif) ligand 5 |
C00001837
C00001889
|
407056 | MIR99B, MIRN99B | microRNA 99b |
C00001889
|
1576 | CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 | cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) |
C00001837
|
3576 | IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 | interleukin 8 |
C00001837
|
3757 | KCNH2, ERG1, HERG, HERG1, Kv11.1, LQT2, SQT1 | potassium voltage-gated channel, subfamily H (eag-related), member 2 |
C00001837
|
207 | AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA | v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) |
C00001889
|
338 | APOB, FLDB, LDLCQ4 | apolipoprotein B |
C00001889
|
10550 | ARL6IP5, DERP11, GTRAP3-18, JWA, PRAF3, addicsin, hp22, jmx | ADP-ribosylation-like factor 6 interacting protein 5 |
C00001889
|
409 | ARRB2, ARB2, ARR2, BARR2 | arrestin, beta 2 |
C00001889
|
578 | BAK1, BAK, BAK-LIKE, BCL2L7, CDN1 | BCL2-antagonist/killer 1 |
C00001889
|
27113 | BBC3, JFY-1, JFY1, PUMA | BCL2 binding component 3 |
C00001889
|
10018 | BCL2L11, BAM, BIM, BOD | BCL2-like 11 (apoptosis facilitator) |
C00001889
|
8678 | BECN1, ATG6, VPS30, beclin1 | beclin 1, autophagy related |
C00001889
|
841 | CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 | caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) |
C00001889
|
6355 | CCL8, HC14, MCP-2, MCP2, SCYA10, SCYA8 | chemokine (C-C motif) ligand 8 |
C00001889
|
1026 | CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 | cyclin-dependent kinase inhibitor 1A (p21, Cip1) |
C00001889
|
8824 | CES2, CE-2, CES2A1, PCE-2, iCE | carboxylesterase 2 (EC:3.1.1.1 3.1.1.84 3.1.1.56) |
C00001889
|
1312 | COMT | catechol-O-methyltransferase (EC:2.1.1.6) |
C00001889
|
1401 | CRP, PTX1 | C-reactive protein, pentraxin-related |
C00001889
|
1643 | DDB2, DDBB, UV-DDB2 | damage-specific DNA binding protein 2, 48kDa |
C00001889
|
1984 | EIF5A, EIF-5A, EIF5A1, eIF5AI | eukaryotic translation initiation factor 5A |
C00001889
|
2155 | F7, SPCA | coagulation factor VII (serum prothrombin conversion accelerator) (EC:3.4.21.21) |
C00001889
|
355 | FAS, ALPS1A, APO-1, APT1, CD95, FAS1, FASTM, TNFRSF6 | Fas cell surface death receptor |
C00001889
|
2247 | FGF2, BFGF, FGF-2, FGFB, HBGF-2 | fibroblast growth factor 2 (basic) |
C00001889
|
3557 | IL1RN, DIRA, ICIL-1RA, IL-1RN, IL-1ra, IL-1ra3, IL1F3, IL1RA, IRAP, MVCD4 | interleukin 1 receptor antagonist |
C00001889
|
3569 | IL6, BSF2, HGF, HSF, IFNB2, IL-6 | interleukin 6 (interferon, beta 2) |
C00001889
|
3725 | JUN, AP-1, AP1, c-Jun | jun proto-oncogene |
C00001889
|
8609 | KLF7, UKLF | Kruppel-like factor 7 (ubiquitous) |
C00001889
|
4010 | LMX1B, LMX1.2, NPS1 | LIM homeobox transcription factor 1, beta |
C00001889
|
5594 | MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk | mitogen-activated protein kinase 1 (EC:2.7.11.24) |
C00001889
|
5595 | MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK | mitogen-activated protein kinase 3 (EC:2.7.11.24) |
C00001889
|
406901 | MIR107, MIRN107, miR-107 | microRNA 107 |
C00001889
|
406921 | MIR132, MIRN132, miRNA132 | microRNA 132 |
C00001889
|
100302258 | MIR1469, MIRN1469, hsa-mir-1469 | microRNA 1469 |
C00001889
|
406938 | MIR146A, MIRN146, MIRN146A, miR-146a, miRNA146A | microRNA 146a |
C00001889
|
406942 | MIR150, MIRN150, miRNA150 | microRNA 150 |
C00001889
|
406947 | MIR155, MIRN155, miRNA155 | microRNA 155 |
C00001889
|
406949 | MIR15B, MIRN15B, hsa-mir-15b, miR-15b | microRNA 15b |
C00001889
|
406966 | MIR191, MIRN191, miR-191 | microRNA 191 |
C00001889
|
100302129 | MIR1915, MIRN1915, hsa-mir-1915 | microRNA 1915 |
C00001889
|
406991 | MIR21, MIRN21, hsa-mir-21, miR-21, miRNA21 | microRNA 21 |
C00001889
|
407006 | MIR221, MIRN221, miRNA221, mir-221 | microRNA 221 |
C00001889
|
407010 | MIR23A, MIRN23A, hsa-mir-23a, miRNA23A | microRNA 23a |
C00001889
|
407011 | MIR23B, MIRN23B, hsa-mir-23b, miRNA23B | microRNA 23b |
C00001889
|
407015 | MIR26A1, MIR26A, MIRN26A1 | microRNA 26a-1 |
C00001889
|
407017 | MIR26B, MIRN26B, hsa-mir-26b, miR-26b | microRNA 26b |
C00001889
|
407037 | MIR320A, MIRN320, MIRN320A, hsa-mir-320a | microRNA 320a |
C00001889
|
494335 | MIR423, MIRN423, hsa-mir-423 | microRNA 423 |
C00001889
|
693223 | MIR638, MIRN638, hsa-mir-638 | microRNA 638 |
C00001889
|
6347 | CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF | chemokine (C-C motif) ligand 2 |
C00001837
|
4792 | NFKBIA, IKBA, MAD-3, NFKBI | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha |
C00001889
|
4814 | NINJ1, NIN1, NINJURIN | ninjurin 1 |
C00001889
|
4985 | OPRD1, OPRD | opioid receptor, delta 1 |
C00001889
|
4988 | OPRM1, LMOR, M-OR-1, MOP, MOR, MOR1, OPRM | opioid receptor, mu 1 |
C00001889
|
5155 | PDGFB, IBGC5, PDGF-2, PDGF2, SIS, SSV, c-sis | platelet-derived growth factor beta polypeptide |
C00001889
|
5443 | POMC, ACTH, CLIP, LPH, MSH, NPP, POC | proopiomelanocortin |
C00001889
|
84152 | PPP1R1B, DARPP-32, DARPP32 | protein phosphatase 1, regulatory (inhibitor) subunit 1B (EC:3.1.3.16) |
C00001889
|
5970 | RELA, NFKB3, p65 | v-rel avian reticuloendotheliosis viral oncogene homolog A |
C00001889
|
6648 | SOD2, IPOB, MNSOD, MVCD6 | superoxide dismutase 2, mitochondrial (EC:1.15.1.1) |
C00001889
|
6778 | STAT6, D12S1644, IL-4-STAT, STAT6B, STAT6C | signal transducer and activator of transcription 6, interleukin-4 induced |
C00001889
|
7099 | TLR4, ARMD10, CD284, TLR-4, TOLL | toll-like receptor 4 |
C00001889
|
7157 | TP53, BCC7, LFS1, P53, TRP53 | tumor protein p53 |
C00001889
|
54658 | UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A | UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) |
C00001889
|
54575 | UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J | UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) |
C00001889
|
54659 | UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C | UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) |
C00001889
|
54578 | UGT1A6, GNT1, HLUGP, HLUGP1, UDPGT, UDPGT_1-6, UGT1, UGT1A6S, UGT1F | UDP glucuronosyltransferase 1 family, polypeptide A6 (EC:2.4.1.17) |
C00001889
|
54576 | UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H | UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) |
C00001889
|
54600 | UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I | UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) |
C00001889
|
7364 | UGT2B7, UDPGT_2B9, UDPGT2B7, UDPGTH2, UGT2B9 | UDP glucuronosyltransferase 2 family, polypeptide B7 (EC:2.4.1.17) |
C00001889
|
OMIM | preferred title | UniProt |
---|---|---|
#614373 | Amyotrophic lateral sclerosis 16, juvenile; als16 |
Q99720
|
#601816 | Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 |
P22309
|
#300615 | Brunner syndrome |
P21397
|
#218800 | Crigler-najjar syndrome, type i |
P22309
P22310 |
#606785 | Crigler-najjar syndrome, type ii |
P22309
P22310 |
#607208 | Dravet syndrome |
P35498
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#613721 | Epileptic encephalopathy, early infantile, 11; eiee11 |
Q99250
|
#604403 | Generalized epilepsy with febrile seizures plus, type 2; gefsp2 |
P35498
|
#143500 | Gilbert syndrome |
P22309
P22310 |
#237900 | Hyperbilirubinemia, transient familial neonatal; hblrtfn |
P22309
|
#612244 | Inflammatory bowel disease 13; ibd13 |
P08183
|
#613688 | Long qt syndrome 2; lqt2 |
Q12809
|
#609634 | Migraine, familial hemiplegic, 3; fhm3 |
P35498
|
#607745 | Seizures, benign familial infantile, 3; bfis3 |
Q99250
|
#609620 | Short qt syndrome 1; sqt1 |
Q12809
|
KEGG | name | UniProt |
---|---|---|
H00036 | Osteosarcoma |
P08684
(marker)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00548 | Brunner syndrome |
P21397
(related)
|
H00208 | Hyperbilirubinemia |
P22309
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00775 | Familial or sporadic hemiplegic migraine |
P35498
(related)
|
H00783 | Febrile seizures |
P35498
(related)
|
H00720 | Long QT syndrome |
Q12809
(related)
|
H00725 | Short QT syndrome |
Q12809
(related)
|
H00606 | Early infantile epileptic encephalopathy |
Q99250
(related)
|
H00806 | Benign familial neonatal and infantile epilepsies |
Q99250
(related)
|
MESH or OMIM | name |
KNApSAcK
metabolite |
---|---|---|
D012640 | Seizures |
C00027603
C00001837 C00001889 |
D004244 | Dizziness |
C00001837
C00001889 |
D015746 | Abdominal Pain |
C00001837
C00001889 |
D013610 | Tachycardia |
C00001837
C00001889 |
D000860 | Anoxia |
C00001837
C00001889 |
D001049 | Apnea |
C00001837
C00001889 |
D013375 | Substance Withdrawal Syndrome |
C00001837
C00001889 |
D001919 | Bradycardia |
C00001837
C00001889 |
D019966 | Substance-Related Disorders |
C00001837
C00001889 |
D002375 | Catalepsy |
C00001837
C00001889 |
D046628 | Sphincter of Oddi Dysfunction |
C00001837
C00001889 |
D003128 | COMA |
C00001837
C00001889 |
D003248 | Constipation |
C00001837
C00001889 |
D003371 | Cough |
C00001837
C00001889 |
D013035 | Spasm |
C00001837
C00001889 |
D003693 | Delirium |
C00001837
C00001889 |
D011537 | Pruritus |
C00001837
C00001889 |
D003967 | Diarrhea |
C00001837
C00001889 |
D014839 | Vomiting |
C00001837
C00001889 |
D011297 | Prenatal Exposure Delayed Effects |
C00001837
C00001889 |
D010149 | Pain, Postoperative |
C00001837
C00001889 |
D010146 | Pain |
C00001837
C00001889 |
D009357 | Neonatal Abstinence Syndrome |
C00001837
C00001889 |
D009325 | Nausea |
C00001837
C00001889 |
D005076 | Exanthema |
C00001837
C00001889 |
D005334 | Fever |
C00001837
C00001889 |
D009207 | Myoclonus |
C00001837
C00001889 |
D005767 | Gastrointestinal Diseases |
C00001837
C00001889 |
D006261 | Headache |
C00001837
C00001889 |
D009120 | Muscle Cramp |
C00001837
C00001889 |
D006930 | Hyperalgesia |
C00001837
C00001889 |
D007674 | Kidney Diseases |
C00001837
C00001889 |
D006973 | Hypertension |
C00001837
C00001889 |
D007008 | Hypokalemia |
C00001837
C00001889 |
D018476 | Hypokinesia |
C00001837
C00001889 |
D007022 | Hypotension |
C00001837
C00001889 |
D007024 | Hypotension, Orthostatic |
C00001837
C00001889 |
D015427 | Reperfusion Injury |
C00001889
|
D006967 | Hypersensitivity |
C00001837
|
D007680 | Kidney Neoplasms |
C00001837
|
D007681 | Kidney Papillary Necrosis |
C00001837
|
D006330 | Heart Defects, Congenital |
C00001837
|
D005494 | Folic Acid Deficiency |
C00001837
|
D053159 | Dysuria |
C00001837
|
D004421 | Dystonia |
C00001837
|
D009461 | Neurologic Manifestations |
C00001837
|
D009771 | Obsessive-Compulsive Disorder |
C00001837
|
D004415 | Dyspepsia |
C00001837
|
D003875 | Drug Eruptions |
C00001837
|
D010195 | Pancreatitis |
C00001837
|
D004310 | Double Outlet Right Ventricle |
C00001837
|
D003866 | Depressive Disorder |
C00001837
|
D011695 | Purpura, Schoenlein-Henoch |
C00001837
|
D011776 | Pyuria |
C00001837
|
D012185 | Retroperitoneal Fibrosis |
C00001837
|
D012216 | Rheumatic Diseases |
C00001837
|
D012871 | Skin Diseases |
C00001837
|
D012891 | Sleep Apnea Syndromes |
C00001837
|
D003490 | Cyanosis |
C00001837
|
D003085 | Colic |
C00001837
|
D020521 | Stroke |
C00001837
|
D002295 | Carcinoma, Transitional Cell |
C00001837
|
D001660 | Biliary Tract Diseases |
C00001837
|
D000740 | Anemia |
C00001837
|
D014517 | Ureteral Obstruction |
C00001837
|
D014806 | Vitamin B 12 Deficiency |
C00001837
|
D009369 | Neoplasms |
C00027603
|
D000014 | Abnormalities, Drug-Induced |
C00001889
|
D000142 | Acidosis, Respiratory |
C00001889
|
D056586 | Acute Chest Syndrome |
C00001889
|
D058186 | Acute Kidney Injury |
C00001889
|
D000219 | Adams-Stokes Syndrome |
C00001889
|
D000307 | Adrenal Gland Diseases |
C00001889
|
D019973 | Alcohol-Related Disorders |
C00001889
|
D000647 | Amnesia |
C00001889
|
D000707 | Anaphylaxis |
C00001889
|
D000855 | Anorexia |
C00001889
|
D001002 | Anuria |
C00001889
|
D001008 | Anxiety Disorders |
C00001889
|
D001145 | Arrhythmias, Cardiac |
C00001889
|
D001281 | Atrial Fibrillation |
C00001889
|
D054537 | Atrioventricular Block |
C00001889
|
D001284 | Atrophy |
C00001889
|
D001416 | Back Pain |
C00001889
|
D001480 | Basal Ganglia Diseases |
C00001889
|
D001714 | Bipolar Disorder |
C00001889
|
D001927 | Brain Diseases |
C00001889
|
D002545 | Brain Ischemia |
C00001889
|
D002056 | Burns |
C00001889
|
D002194 | Capgras Syndrome |
C00001889
|
D002311 | Cardiomyopathy, Dilated |
C00001889
|
D002389 | Catatonia |
C00001889
|
D002637 | Chest Pain |
C00001889
|
D002764 | Cholecystitis |
C00001889
|
D002769 | Cholelithiasis |
C00001889
|
D002779 | Cholestasis |
C00001889
|
D003072 | Cognition Disorders |
C00001889
|
D003110 | Colonic Neoplasms |
C00001889
|
D003137 | Common Bile Duct Diseases |
C00001889
|
D020918 | Complex Regional Pain Syndromes |
C00001889
|
D003221 | Confusion |
C00001889
|
D003244 | Consciousness Disorders |
C00001889
|
D003327 | Coronary Disease |
C00001889
|
D055191 | Delayed Emergence from Anesthesia |
C00001889
|
D003731 | Dental Caries |
C00001889
|
D003919 | Diabetes Insipidus |
C00001889
|
D004108 | Dilatation, Pathologic |
C00001889
|
D004172 | Diplopia |
C00001889
|
D018450 | Disease Progression |
C00001889
|
D006970 | Disorders of Excessive Somnolence |
C00001889
|
D004213 | Dissociative Disorders |
C00001889
|
D004342 | Drug Hypersensitivity |
C00001889
|
D056486 | Drug-Induced Liver Injury |
C00001889
|
D062787 | Drug Overdose |
C00001889
|
D064420 | Drug-Related Side Effects and Adverse Reactions |
C00001889
|
D004409 | Dyskinesia, Drug-Induced |
C00001889
|
D004417 | Dyspnea |
C00001889
|
D004487 | Edema |
C00001889
|
D004673 | Encephalomyelitis, Acute Disseminated |
C00001889
|
D004831 | Epilepsies, Myoclonic |
C00001889
|
D004827 | Epilepsy |
C00001889
|
D004830 | Epilepsy, Tonic-Clonic |
C00001889
|
D005094 | Exophthalmos |
C00001889
|
D005157 | Facial Pain |
C00001889
|
D005221 | Fatigue |
C00001889
|
D005242 | Fecal Incontinence |
C00001889
|
D042882 | Gallstones |
C00001889
|
D006099 | Granuloma |
C00001889
|
D006212 | Hallucinations |
C00001889
|
D006331 | Heart Diseases |
C00001889
|
D006417 | Hematuria |
C00001889
|
D006429 | Hemiplegia |
C00001889
|
D006470 | Hemorrhage |
C00001889
|
D006501 | Hepatic Encephalopathy |
C00001889
|
D006526 | Hepatitis C |
C00001889
|
D006556 | Heroin Dependence |
C00001889
|
D006560 | Herpes Labialis |
C00001889
|
D006606 | Hiccup |
C00001889
|
D006819 | Hyaline Membrane Disease |
C00001889
|
D006869 | Hydronephrosis |
C00001889
|
D006935 | Hypercapnia |
C00001889
|
D006940 | Hyperemia |
C00001889
|
D006941 | Hyperesthesia |
C00001889
|
D006948 | Hyperkinesis |
C00001889
|
D006987 | Hypesthesia |
C00001889
|
D007006 | Hypogonadism |
C00001889
|
D007018 | Hypopituitarism |
C00001889
|
D007035 | Hypothermia |
C00001889
|
D002534 | Hypoxia, Brain |
C00001889
|
D019586 | Intracranial Hypertension |
C00001889
|
D048949 | Labor Pain |
C00001889
|
D007826 | Laryngismus |
C00001889
|
D007859 | Learning Disorders |
C00001889
|
D053609 | Lethargy |
C00001889
|
D017116 | Low Back Pain |
C00001889
|
D008175 | Lung Neoplasms |
C00001889
|
D008305 | Malignant Hyperthermia |
C00001889
|
D008569 | Memory Disorders |
C00001889
|
D015877 | Miosis |
C00001889
|
D009021 | Morphine Dependence |
C00001889
|
D009069 | Movement Disorders |
C00001889
|
D052016 | Mucositis |
C00001889
|
D009122 | Muscle Hypertonia |
C00001889
|
D009123 | Muscle Hypotonia |
C00001889
|
D009127 | Muscle Rigidity |
C00001889
|
D009128 | Muscle Spasticity |
C00001889
|
D018908 | Muscle Weakness |
C00001889
|
D015878 | Mydriasis |
C00001889
|
D009203 | Myocardial Infarction |
C00001889
|
D017202 | Myocardial Ischemia |
C00001889
|
D015428 | Myocardial Reperfusion Injury |
C00001889
|
D009290 | Narcolepsy |
C00001889
|
D009336 | Necrosis |
C00001889
|
D009422 | Nervous System Diseases |
C00001889
|
D009437 | Neuralgia |
C00001889
|
D009436 | Neural Tube Defects |
C00001889
|
D020258 | Neurotoxicity Syndromes |
C00001889
|
D009759 | Nystagmus, Pathologic |
C00001889
|
D009846 | Oliguria |
C00001889
|
D009293 | Opioid-Related Disorders |
C00001889
|
D010148 | Pain, Intractable |
C00001889
|
D010243 | Paralysis |
C00001889
|
D010259 | Paranoid Disorders |
C00001889
|
D020335 | Paraparesis |
C00001889
|
D020336 | Paraparesis, Spastic |
C00001889
|
D010291 | Paresis |
C00001889
|
D010523 | Peripheral Nervous System Diseases |
C00001889
|
D010538 | Peritonitis |
C00001889
|
D010554 | Personality Disorders |
C00001889
|
D020250 | Postoperative Nausea and Vomiting |
C00001889
|
D011595 | Psychomotor Agitation |
C00001889
|
D011596 | Psychomotor Disorders |
C00001889
|
D011605 | Psychoses, Substance-Induced |
C00001889
|
D011654 | Pulmonary Edema |
C00001889
|
D011681 | Pupil Disorders |
C00001889
|
D012021 | Reflex, Abnormal |
C00001889
|
D001405 | Reflex, Babinski |
C00001889
|
D051437 | Renal Insufficiency |
C00001889
|
D007232 | Infant, Newborn, Diseases |
C00001837
|
D012120 | Respiration Disorders |
C00001889
|
D012131 | Respiratory Insufficiency |
C00001889
|
D012206 | Rhabdomyolysis |
C00001889
|
D012585 | Sciatica |
C00001889
|
D012769 | Shock |
C00001889
|
D020182 | Sleep Apnea, Central |
C00001889
|
D020181 | Sleep Apnea, Obstructive |
C00001889
|
D012892 | Sleep Deprivation |
C00001889
|
D012893 | Sleep Disorders |
C00001889
|
D013064 | Speech Disorders |
C00001889
|
D013117 | Spinal Cord Compression |
C00001889
|
D013118 | Spinal Cord Diseases |
C00001889
|
D013203 | Staphylococcal Infections |
C00001889
|
D013226 | Status Epilepticus |
C00001889
|
D019956 | Stereotypic Movement Disorder |
C00001889
|
D053608 | Stupor |
C00001889
|
D013705 | Temporomandibular Joint Disorders |
C00001889
|
D018677 | Tooth Injuries |
C00001889
|
D016388 | Tooth Loss |
C00001889
|
D014474 | Unconsciousness |
C00001889
|
D053201 | Urinary Bladder, Overactive |
C00001889
|
D014549 | Urinary Incontinence |
C00001889
|
D016055 | Urinary Retention |
C00001889
|
D014555 | Urination Disorders |
C00001889
|
D018487 | Ventricular Dysfunction, Left |
C00001889
|
D018879 | Ventricular Premature Complexes |
C00001889
|
D014717 | Vertigo |
C00001889
|
D014786 | Vision Disorders |
C00001889
|
D015431 | Weight Loss |
C00001889
|
D014987 | Xerostomia |
C00001889
|