KCF-S cluster No. 4235 (3 metabolites)

Corresponding Phytochemical cluster No. 4


Plant Species


Cumulative plant class count

class name count
eudicotyledons 5

Cumulative family count

class name count
Papaveraceae 5

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Isoquinoline alkaloids 3

metabolites link (3)

br08003 Category KEGG ID KNApSAcK ID
Isoquinoline alkaloids C06174 C00001837
Isoquinoline alkaloids C01516 C00001889
Isoquinoline alkaloids C06171 C00027603

Metabolite list (3)

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 External link 512 Codeine
/ (-)-Codeine
CHEMBL485
CHEMBL22662
CHEMBL612012
CHEMBL1907378
D003061
16 / 12 / 6 6 / 66
C00001889 External link 512 Morphine
/ (-)-Morphine
CHEMBL70
CHEMBL1888905
CHEMBL2133708
CHEMBL2139208
D009020
32 / 17 / 11 71 / 199
C00027603 External link 512 6-Oxocodeine
/ (-)-Codeinone
CHEMBL163490
CHEMBL257627
C046414
1 / 0 / 0 5 / 2

Human Protein / Gene in interactions

32 ChEMBL Protein in interactions

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

75 Gene in CTD interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (17)

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 DISEASE (11)

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)

Diseases related to CTD interactions

229 disease in interactions with metabolites

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