KCF-S cluster No. 1378 (7 metabolites)

Corresponding Phytochemical cluster No. 7


Plant Species


Cumulative plant class count

class name count
asterids 19

Cumulative family count

class name count
Rubiaceae 16
Oleaceae 2
Apocynaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Quinoline alkaloids 3

metabolites link (3)

br08003 Category KEGG ID KNApSAcK ID
Quinoline alkaloids C11379 C00002147
Quinoline alkaloids C10696 C00002173
Quinoline alkaloids C06527 C00031117

Metabolite list (7)

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
C00002147 External link 512 Cinchonidine
CHEMBL15134
CHEMBL461234
CHEMBL518804
CHEMBL533841
CHEMBL588619
CHEMBL611480
CHEMBL1414315
CHEMBL1477170
CHEMBL1590546
CHEMBL2079612
CHEMBL2357353
C041622
13 / 10 / 8
C00002173 External link 512 Hydroquinidine
CHEMBL531471
CHEMBL531472
CHEMBL588934
CHEMBL602767
CHEMBL1436416
CHEMBL1531111
CHEMBL1617471
CHEMBL1740727
CHEMBL1906890
CHEMBL2079611
CHEMBL2092739
CHEMBL2305514
CHEMBL2355802
C014486
9 / 12 / 15 0 / 4
C00002193 External link 512 Quinine
CHEMBL97
CHEMBL15088
CHEMBL21578
CHEMBL1294
CHEMBL170
CHEMBL387326
CHEMBL407725
CHEMBL512340
CHEMBL522505
CHEMBL460606
CHEMBL601807
CHEMBL576997
CHEMBL1358565
CHEMBL1364159
CHEMBL1616938
CHEMBL1741006
CHEMBL1878119
CHEMBL2355467
D011803
48 / 55 / 40 18 / 83
C00026411 External link 512 Cupreine
/ Ultraquinine
/ Desmethylquinine
/ O-Demethylquinine
/ O6'-Demethylquinine
C029819
C00026417 External link 512 Hydrocupreine
/ Dihydrocupreine
/ 10,11-Dihydrocupreine
/ O6'-Demethylhydroquinine
/ 6'-Hydroxydihydrocinchonidine
CHEMBL532678
CHEMBL587165
C029820
C00026466 External link 512 N-Methyldihydroquinicinol
C00031117 External link 512 Quinidine
/ (+)-Quinidine
CHEMBL97
CHEMBL15088
CHEMBL21578
CHEMBL1294
CHEMBL170
CHEMBL387326
CHEMBL407725
CHEMBL512340
CHEMBL522505
CHEMBL460606
CHEMBL601807
CHEMBL576997
CHEMBL1358565
CHEMBL1364159
CHEMBL1616938
CHEMBL1741006
CHEMBL1878119
CHEMBL2355467
D011802
48 / 55 / 40 28 / 83

Human Protein / Gene in interactions

51 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002147 C00002173 C00002193 C00031117 1 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00002147 C00002173 C00002193 C00031117 3 / 2
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002147 C00002173 C00002193 C00031117 0 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002173 C00002193 C00031117 3 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002147 C00002193 C00031117 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002147 C00002193 C00031117 0 / 0
O00255 Menin Unclassified protein C00002173 C00002193 C00031117 2 / 5
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002147 C00002193 C00031117 1 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002173 C00002193 C00031117 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002147 C00002193 C00031117 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002173 C00002193 C00031117 1 / 2
P83916 Chromobox protein homolog 1 Unclassified protein C00002147 C00002193 C00031117 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002147 C00002193 C00031117 0 / 0
O75496 Geminin Unclassified protein C00002147 C00002193 C00031117 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002147 C00002193 C00031117 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00002173 C00002193 C00031117 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00002193 C00031117 0 / 0
P08183 Multidrug resistance protein 1 drug C00002193 C00031117 1 / 0
Q8TCC7 Solute carrier family 22 member 8 Antiporter C00002193 C00031117 0 / 0
P46721 Solute carrier organic anion transporter family member 1A2 Unclassified protein C00002193 C00031117 0 / 0
P02768 Serum albumin Secreted protein C00002193 C00031117 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00002193 C00031117 3 / 1
Q9NPD5 Solute carrier organic anion transporter family member 1B3 Electrochemical transporter C00002193 C00031117 1 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00002193 C00031117 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002193 C00031117 5 / 3
Q9NY46 Sodium channel protein type 3 subunit alpha SCN alpha, NaV1.x C00002193 C00031117 0 / 0
P37840 Alpha-synuclein Unclassified protein C00002193 C00031117 4 / 2
O15245 Solute carrier family 22 member 1 Drug uniporter C00002193 C00031117 0 / 0
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein C00002193 C00031117 1 / 1
P35498 Sodium channel protein type 1 subunit alpha SCN alpha, NaV1.x C00002193 C00031117 3 / 2
Q86VL8 Multidrug and toxin extrusion protein 2 Cation antiporter C00002193 C00031117 0 / 0
Q14524 Sodium channel protein type 5 subunit alpha SCN alpha, NaV1.x C00002193 C00031117 9 / 7
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00002193 C00031117 2 / 2
O95342 Bile salt export pump drug C00002193 C00031117 2 / 1
Q99700 Ataxin-2 Unclassified protein C00002193 C00031117 1 / 1
Q99250 Sodium channel protein type 2 subunit alpha SCN alpha, NaV1.x C00002193 C00031117 2 / 2
Q96FL8 Multidrug and toxin extrusion protein 1 Cation antiporter C00002193 C00031117 0 / 0
P22460 Potassium voltage-gated channel subfamily A member 5 KCNA, Kv1.x (Shaker) C00002193 C00031117 1 / 1
P04156 Major prion protein Surface antigen C00002193 C00031117 6 / 2
Q9UBT6 DNA polymerase kappa Enzyme C00002193 C00031117 0 / 0
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00002193 C00031117 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002193 C00031117 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002193 C00031117 1 / 1
O15244 Solute carrier family 22 member 2 Drug uniporter C00002193 C00031117 0 / 0
Q9Y6L6 Solute carrier organic anion transporter family member 1B1 Electrochemical transporter C00002193 C00031117 1 / 0
Q9H015 Solute carrier family 22 member 4 Unclassified protein C00002193 C00031117 1 / 1
O76082 Solute carrier family 22 member 5 Unclassified protein C00002193 C00031117 1 / 2
P06276 Cholinesterase Hydrolase C00002193 C00031117 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002147 4 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002173 2 / 2
Q13148 TAR DNA-binding protein 43 Unclassified protein C00002147 1 / 1

34 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00002193 C00031117
6581 SLC22A3, EMT, EMTH, OCT3 solute carrier family 22 (organic cation transporter), member 3 C00002193 C00031117
6582 SLC22A2, OCT2 solute carrier family 22 (organic cation transporter), member 2 C00002193 C00031117
6580 SLC22A1, HOCT1, OCT1, oct1_cds solute carrier family 22 (organic cation transporter), member 1 C00002193 C00031117
338567 KCNK18, K2p18.1, MGR13, TRESK, TRESK-2, TRESK2, TRIK potassium channel, subfamily K, member 18 C00002193 C00031117
3757 KCNH2, ERG1, HERG, HERG1, Kv11.1, LQT2, SQT1 potassium voltage-gated channel, subfamily H (eag-related), member 2 C00002193 C00031117
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00002193 C00031117
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002193 C00031117
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00002193 C00031117
1557 CYP2C19, CPCJ, CYP2C, P450C2C, P450IIC19 cytochrome P450, family 2, subfamily C, polypeptide 19 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00002193 C00031117
2944 GSTM1, GST1, GSTM1-1, GSTM1a-1a, GSTM1b-1b, GTH4, GTM1, H-B, MU, MU-1 glutathione S-transferase mu 1 (EC:2.5.1.18) C00002193 C00031117
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) C00002193 C00031117
3756 KCNH1, EAG, EAG1, Kv10.1, h-eag potassium voltage-gated channel, subfamily H (eag-related), member 1 C00031117
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) C00031117
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00031117
3479 IGF1, IGF-I, IGF1A, IGFI insulin-like growth factor 1 (somatomedin C) C00031117
83729 INHBE inhibin, beta E C00031117
2168 FABP1, FABPL, L-FABP fatty acid binding protein 1, liver C00031117
11067 C10orf10, DEPP, FIG chromosome 10 open reading frame 10 C00031117
440 ASNS, TS11 asparagine synthetase (glutamine-hydrolyzing) (EC:6.3.5.4) C00031117
26471 NUPR1, COM1, P8 nuclear protein, transcriptional regulator, 1 C00031117
146 ADRA1D, ADRA1, ADRA1A, ADRA1R, ALPHA1, DAR, dJ779E11.2 adrenoceptor alpha 1D C00031117
147 ADRA1B, ADRA1, ALPHA1BAR adrenoceptor alpha 1B C00031117
148 ADRA1A, ADRA1C, ADRA1L1, ALPHA1AAR adrenoceptor alpha 1A C00031117
6515 SLC2A3, GLUT3 solute carrier family 2 (facilitated glucose transporter), member 3 C00031117
55244 SLC47A1, MATE1 solute carrier family 47 (multidrug and toxin extrusion), member 1 C00031117
6876 TAGLN, SM22, SMCC, TAGLN1, WS3-10 transgelin C00031117
943 TNFRSF8, CD30, D1S166E, Ki-1 tumor necrosis factor receptor superfamily, member 8 C00031117
351 APP, AAA, ABETA, ABPP, AD1, APPI, CTFgamma, CVAP, PN-II, PN2 amyloid beta (A4) precursor protein C00002193
1559 CYP2C9, CPC9, CYP2C, CYP2C10, CYPIIC9, P450IIC9 cytochrome P450, family 2, subfamily C, polypeptide 9 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00002193
3552 IL1A, IL-1A, IL1, IL1-ALPHA, IL1F1 interleukin 1, alpha C00002193
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00002193
84679 SLC9A7, NHE-7, NHE7, SLC9A6 solute carrier family 9, subfamily A (NHE7, cation proton antiporter 7), member 7 C00002193
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00002193

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (62)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614022 Atrial fibrillation, familial, 10; atfb10 Q14524
#612240 Atrial fibrillation, familial, 7; atfb7 P22460
#108770 Atrial standstill Q14524
%606641 Body mass index; bmi P37231
#601144 Brugada syndrome 1; brgda1 Q14524
#601154 Cardiomyopathy, dilated, 1e; cmd1e Q14524
#212140 Carnitine deficiency, systemic primary; cdsp O76082
#609338 Carotid intimal medial thickness 1 P37231
#605479 Cholestasis, benign recurrent intrahepatic, 2; bric2 O95342
#601847 Cholestasis, progressive familial intrahepatic, 2; pfic2 O95342
#123400 Creutzfeldt-jakob disease; cjd P04156
#127750 Dementia, lewy body; dlb P37840
#119900 Digital clubbing, isolated congenital P15428
#607208 Dravet syndrome P35498
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#237500 Dubin-johnson syndrome; djs Q92887
#613721 Epileptic encephalopathy, early infantile, 11; eiee11 Q99250
#600072 Fatal familial insomnia; ffi P04156
#600274 Frontotemporal dementia; ftd P10636
#604403 Generalized epilepsy with febrile seizures plus, type 2; gefsp2 P35498
#137440 Gerstmann-straussler disease; gsd P04156
#137800 Glioma susceptibility 1; glm1 P37231
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#603218 Huntington disease-like 1; hdl1 P04156
#237450 Hyperbilirubinemia, rotor type; hblrr Q9NPD5
Q9Y6L6
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#245300 Kuru, susceptibility to P04156
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613688 Long qt syndrome 2; lqt2 Q12809
#603830 Long qt syndrome 3; lqt3 Q14524
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#609634 Migraine, familial hemiplegic, 3; fhm3 P35498
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#601665 Obesity P37231
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#113900 Progressive familial heart block, type ia; pfhb1a Q14524
#180300 Rheumatoid arthritis; ra Q9H015
#607745 Seizures, benign familial infantile, 3; bfis3 Q99250
#609620 Short qt syndrome 1; sqt1 Q12809
#608567 Sick sinus syndrome 1, autosomal recessive; sss1 Q14524
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#606688 Spongiform encephalopathy with neuropsychiatric features P04156
#272120 Sudden infant death syndrome Q14524
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#603829 Ventricular fibrillation during myocardial infarction, susceptibility to Q14524

KEGG DISEASE (45)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00286 Crohn's disease O76082 (related)
Q9H015 (related)
H00525 Disorders of fatty-acid oxidation O76082 (related)
H00624 Familial cholestasis O95342 (related)
H00061 Prion diseases P04156 (related)
H01243 Huntington's disease-like syndrome P04156 (related)
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00731 Atrial fibrillation P22460 (related)
Q14524 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00775 Familial or sporadic hemiplegic migraine P35498 (related)
H00783 Febrile seizures P35498 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00720 Long QT syndrome Q12809 (related)
Q14524 (related)
H00725 Short QT syndrome Q12809 (related)
H00294 Dilated cardiomyopathy (DCM) Q14524 (related)
H00728 Brugada syndrome (BRS) Q14524 (related)
H00729 Sick sinus syndrome (SSS) Q14524 (related)
H00730 Familial idiopathic ventricular fibrillation Q14524 (related)
H01263 Progressive cardiac conduction defect (PCCD) Q14524 (related)
H00208 Hyperbilirubinemia Q92887 (related)
H00606 Early infantile epileptic encephalopathy Q99250 (related)
H00806 Benign familial neonatal and infantile epilepsies Q99250 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)

Diseases related to CTD interactions

138 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006099 Granuloma C00002173
C00031117
C00002193
D006505 Hepatitis C00002173
C00031117
C00002193
D013610 Tachycardia C00031117
C00002193
D014786 Vision Disorders C00031117
C00002193
D058186 Acute Kidney Injury C00031117
C00002193
D000380 Agranulocytosis C00031117
C00002193
D018879 Ventricular Premature Complexes C00031117
C00002193
D000743 Anemia, Hemolytic C00031117
C00002193
D014693 Ventricular Fibrillation C00031117
C00002193
D001145 Arrhythmias, Cardiac C00031117
C00002193
D014657 Vasculitis C00031117
C00002193
D016171 Torsades de Pointes C00031117
C00002193
D013921 Thrombocytopenia C00031117
C00002193
D054537 Atrioventricular Block C00031117
C00002193
D001919 Bradycardia C00031117
C00002193
D064420 Drug-Related Side Effects and Adverse Reactions C00002173
C00031117
D013575 Syncope C00031117
C00002193
D011618 Psychotic Disorders C00031117
C00002193
D010787 Photosensitivity Disorders C00031117
C00002193
D016778 Malaria, Falciparum C00031117
C00002193
D008288 Malaria C00031117
C00002193
D008133 Long QT Syndrome C00031117
C00002193
D003638 Deafness C00031117
C00002193
D007024 Hypotension, Orthostatic C00031117
C00002193
D007022 Hypotension C00031117
C00002193
D007008 Hypokalemia C00031117
C00002193
D034381 Hearing Loss C00031117
C00002193
D003875 Drug Eruptions C00031117
C00002193
D005334 Fever C00031117
C00002193
D056486 Drug-Induced Liver Injury C00031117
C00002193
D005315 Fetal Diseases C00002193
D004342 Drug Hypersensitivity C00031117
D005767 Gastrointestinal Diseases C00031117
D003967 Diarrhea C00031117
D006323 Heart Arrest C00031117
D006327 Heart Block C00031117
D006333 Heart Failure C00031117
D006417 Hematuria C00031117
D006529 Hepatomegaly C00031117
D003704 Dementia C00031117
D003693 Delirium C00031117
D016757 Death, Sudden, Cardiac C00031117
D007674 Kidney Diseases C00031117
D007970 Leukopenia C00031117
D054068 Livedo Reticularis C00031117
D023921 Coronary Stenosis C00031117
D008180 Lupus Erythematosus, Systemic C00031117
D008181 Lupus Nephritis C00031117
D008206 Lymphatic Diseases C00031117
D003324 Coronary Artery Disease C00031117
D003117 Color Vision Defects C00031117
D019964 Mood Disorders C00031117
D009103 Multiple Sclerosis C00031117
D018908 Muscle Weakness C00031117
D009325 Nausea C00031117
D009404 Nephrotic Syndrome C00031117
D019954 Neurobehavioral Manifestations C00031117
D010259 Paranoid Disorders C00031117
D010291 Paresis C00031117
D003072 Cognition Disorders C00031117
D015267 Churg-Strauss Syndrome C00031117
D011693 Purpura C00031117
D011695 Purpura, Schoenlein-Henoch C00031117
D011696 Purpura, Thrombocytopenic C00031117
D012131 Respiratory Insufficiency C00031117
D012848 Sinoatrial Block C00031117
D054138 Sinus Arrest, Cardiac C00031117
D013163 Splenomegaly C00031117
D002779 Cholestasis C00031117
D002493 Central Nervous System Diseases C00031117
D013617 Tachycardia, Supraventricular C00031117
D017180 Tachycardia, Ventricular C00031117
D001282 Atrial Flutter C00031117
D001281 Atrial Fibrillation C00031117
D014581 Urticaria C00031117
D014605 Uveitis C00031117
D001168 Arthritis C00031117
D018366 Vasculitis, Leukocytoclastic, Cutaneous C00031117
D018754 Ventricular Dysfunction C00031117
D000744 Anemia, Hemolytic, Autoimmune C00031117
D054141 Ventricular Flutter C00031117
D000741 Anemia, Aplastic C00031117
D007565 Jaundice C00002173
D014927 Wolff-Parkinson-White Syndrome C00031117
D015746 Abdominal Pain C00002193
D000014 Abnormalities, Drug-Induced C00002193
D000550 Amblyopia C00002193
D000855 Anorexia C00002193
D001008 Anxiety Disorders C00002193
D001766 Blindness C00002193
D001943 Breast Neoplasms C00002193
D002637 Chest Pain C00002193
D016770 Ciliophora Infections C00002193
D003128 COMA C00002193
D003221 Confusion C00002193
D003872 Dermatitis C00002193
D004195 Disease Models, Animal C00002193
D004211 Disseminated Intravascular Coagulation C00002193
D004244 Dizziness C00002193
D062787 Drug Overdose C00002193
D004417 Dyspnea C00002193
D004421 Dystonia C00002193
D004830 Epilepsy, Tonic-Clonic C00002193
D005076 Exanthema C00031117
D005393 Fish Diseases C00002193
D006261 Headache C00002193
D006311 Hearing Disorders C00002193
D006319 Hearing Loss, Sensorineural C00002193
D006331 Heart Diseases C00002193
D006461 Hemolysis C00002193
D006463 Hemolytic-Uremic Syndrome C00002193
D006470 Hemorrhage C00002193
D006948 Hyperkinesis C00002193
D007673 Kidney Cortex Necrosis C00002193
D008269 Macular Edema C00002193
D016779 Malaria, Cerebral C00002193
D009120 Muscle Cramp C00002193
D009224 Myotonia Congenita C00002193
D009336 Necrosis C00002193
D009395 Nephritis, Interstitial C00002193
D009468 Neuromuscular Diseases C00002193
D009503 Neutropenia C00002193
D009896 Optic Atrophy C00002193
D009901 Optic Nerve Diseases C00002193
D010146 Pain C00002193
D010198 Pancytopenia C00002193
D018512 Parasitemia C00002193
D011041 Poisoning C00002193
D011697 Purpura, Thrombotic Thrombocytopenic C00002193
D051437 Renal Insufficiency C00002193
D012164 Retinal Diseases C00002193
D012206 Rhabdomyolysis C00002193
D012640 Seizures C00002193
D020922 Sleep-Wake Transition Disorders C00002193
D057049 Thrombotic Microangiopathies C00002193
D014012 Tinnitus C00002193
D015845 Tonic Pupil C00002193
D014839 Vomiting C00002193