Plant Species


Cumulative plant class count

class name count
rosids 2

Cumulative family count

class name count
Fabaceae 2

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (2)

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
C00042226 External link 512 Amphetamine
CHEMBL405
CHEMBL19393
CHEMBL612
D000661
10 / 7 / 4 32 / 144
C00042732 External link 512 Methamphetamine
/ (+)-Methamphetamine
CHEMBL1201201
CHEMBL1927030
D008694
8 / 4 / 5 95 / 172

Human Protein / Gene in interactions

15 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O76082 Solute carrier family 22 member 5 Unclassified protein C00042226 C00042732 1 / 2
Q96RJ0 Trace amine-associated receptor 1 Trace amine receptor C00042226 C00042732 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00042226 C00042732 1 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00042226 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00042732 0 / 1
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00042226 0 / 0
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00042226 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00042226 1 / 1
P31645 Sodium-dependent serotonin transporter Serotonin C00042226 2 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00042732 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00042732 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00042732 0 / 1
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00042226 0 / 0
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00042226 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00042732 1 / 0

113 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
135 ADORA2A, A2aR, ADORA2, RDC8 adenosine A2a receptor C00042226 C00042732
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00042226 C00042732
847 CAT catalase (EC:1.11.1.6) C00042226 C00042732
6647 SOD1, ALS, ALS1, IPOA, SOD, hSod1, homodimer superoxide dismutase 1, soluble (EC:1.15.1.1) C00042226 C00042732
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00042226 C00042732
6531 SLC6A3, DAT, DAT1, PKDYS solute carrier family 6 (neurotransmitter transporter), member 3 C00042226 C00042732
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) C00042226 C00042732
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) C00042226 C00042732
1813 DRD2, D2DR, D2R dopamine receptor D2 C00042226 C00042732
6530 SLC6A2, NAT1, NET, NET1, SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 2 C00042226 C00042732
3725 JUN, AP-1, AP1, c-Jun jun proto-oncogene C00042226 C00042732
2566 GABRG2, CAE2, ECA2, GEFSP3 gamma-aminobutyric acid (GABA) A receptor, gamma 2 C00042226 C00042732
2554 GABRA1, ECA4, EJM, EJM5 gamma-aminobutyric acid (GABA) A receptor, alpha 1 C00042226 C00042732
9568 GABBR2, GABABR2, GPR51, GPRC3B, HG20, HRIHFB2099 gamma-aminobutyric acid (GABA) B receptor, 2 C00042226 C00042732
9463 PICK1, PICK, PRKCABP protein interacting with PRKCA 1 C00042732
2355 FOSL2, FRA2 FOS-like antigen 2 C00042226
2354 FOSB, AP-1, G0S3, GOS3, GOSB FBJ murine osteosarcoma viral oncogene homolog B C00042226
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00042226
2166 FAAH, FAAH-1, PSAB fatty acid amide hydrolase (EC:3.5.1.99) C00042226
2670 GFAP glial fibrillary acidic protein C00042226
692548 C00042226
2152 F3, CD142, TF, TFA coagulation factor III (thromboplastin, tissue factor) C00042226
3726 JUNB, AP-1 jun B proto-oncogene C00042226
3727 JUND, AP-1 jun D proto-oncogene C00042226
4129 MAOB monoamine oxidase B (EC:1.4.3.4) C00042226
8856 NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR nuclear receptor subfamily 1, group I, member 2 C00042226
5179 PENK proenkephalin C00042226
2147 F2, PT, RPRGL2, THPH1 coagulation factor II (thrombin) (EC:3.4.21.5) C00042226
1555 CYP2B6, CPB6, CYP2B, CYP2B7, CYP2B7P, CYPIIB6, EFVM, IIB1, P450 cytochrome P450, family 2, subfamily B, polypeptide 6 (EC:1.14.14.1) C00042226
1454 CSNK1E, CKIepsilon, HCKIE casein kinase 1, epsilon (EC:2.7.11.1) C00042226
7035 TFPI, EPI, LACI, TFI, TFPI1 tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor) C00042226
250 ALPP, ALP, PALP, PLAP, PLAP-1 alkaline phosphatase, placental (EC:3.1.3.1) C00042226
23305 ACSL6, ACS2, FACL6, LACS_6, LACS2, LACS5 acyl-CoA synthetase long-chain family member 6 (EC:6.2.1.3) C00042732
26289 AK5, AK6 adenylate kinase 5 (EC:2.7.4.3 2.7.4.6) C00042732
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00042732
313 AOAH acyloxyacyl hydrolase (neutrophil) (EC:3.1.1.77) C00042732
409 ARRB2, ARB2, ARR2, BARR2 arrestin, beta 2 C00042732
23245 ASTN2, bA67K19.1 astrotactin 2 C00042732
627 BDNF, ANON2, BULN2 brain-derived neurotrophic factor C00042732
54535 CCHCR1, C6orf18, HCR, SBP coiled-coil alpha-helical rod protein 1 C00042732
1604 CD55, CR, CROM, DAF, TC CD55 molecule, decay accelerating factor for complement (Cromer blood group) C00042732
1012 CDH13, CDHH, P105 cadherin 13 (EC:3.6.1.3) C00042732
1061 C00042732
1103 CHAT, CHOACTASE, CMS1A, CMS1A2 choline O-acetyltransferase (EC:2.3.1.6) C00042732
340267 COL28A1, COL28 collagen, type XXVIII, alpha 1 C00042732
1312 COMT catechol-O-methyltransferase (EC:2.1.1.6) C00042732
64478 CSMD1, PPP1R24 CUB and Sushi multiple domains 1 C00042732
8029 CUBN, IFCR, MGA1, gp280 cubilin (intrinsic factor-cobalamin receptor) C00042732
171522 C00042732
1571 CYP2E1, CPE1, CYP2E, P450-J, P450C2E cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) C00042732
81501 DCSTAMP, FIND, TM7SF4, hDC-STAMP dendrocyte expressed seven transmembrane protein C00042732
1812 DRD1, DADR, DRD1A dopamine receptor D1 C00042732
1814 DRD3, D3DR, ETM1, FET1 dopamine receptor D3 C00042732
1815 DRD4, D4DR dopamine receptor D4 C00042732
1978 EIF4EBP1, 4E-BP1, 4EBP1, BP-1, PHAS-I eukaryotic translation initiation factor 4E binding protein 1 C00042732
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00042732
2272 FHIT, AP3Aase, FRA3B fragile histidine triad (EC:3.6.1.29) C00042732
23307 FKBP15, FKBP133, KIAA0674, PPP1R76 FK506 binding protein 15, 133kDa (EC:5.2.1.8) C00042732
2912 GRM2, GLUR2, GPRC1B, MGLUR2, mGlu2 glutamate receptor, metabotropic 2 C00042732
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) C00042732
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00042732
2952 GSTT1 glutathione S-transferase theta 1 (EC:2.5.1.18) C00042732
9951 HS3ST4, 3-OST-4, 30ST4, 3OST4, h3-OST-4 heparan sulfate (glucosamine) 3-O-sulfotransferase 4 (EC:2.8.2.23) C00042732
3350 HTR1A, 5-HT-1A, 5-HT1A, 5HT1a, ADRB2RL1, ADRBRL1, G-21, PFMCD 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled C00042732
3362 HTR6, 5-HT6, 5-HT6R 5-hydroxytryptamine (serotonin) receptor 6, G protein-coupled C00042732
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00042732
9215 LARGE, MDC1D, MDDGA6, MDDGB6 like-glycosyltransferase C00042732
158038 LINGO2, LERN3, LRRN6C leucine rich repeat and Ig domain containing 2 C00042732
5607 MAP2K5, HsT17454, MAPKK5, MEK5, PRKMK5 mitogen-activated protein kinase kinase 5 (EC:2.7.12.2) C00042732
64757 MARC1, MOSC1 mitochondrial amidoxime reducing component 1 C00042732
54996 MARC2, MOSC2, RP11-270A6.1 mitochondrial amidoxime reducing component 2 C00042732
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00042732
4502 MT2A, MT2 metallothionein 2A C00042732
2475 MTOR, FRAP, FRAP1, FRAP2, RAFT1, RAPT1 mechanistic target of rapamycin (serine/threonine kinase) (EC:2.7.11.1) C00042732
4645 MYO5B myosin VB C00042732
4790 NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 C00042732
4886 NPY1R, NPY1-R, NPYR neuropeptide Y receptor Y1 C00042732
3084 NRG1, ARIA, GGF, GGF2, HGL, HRG, HRG1, HRGA, MST131, NDF, SMDF neuregulin 1 C00042732
4988 OPRM1, LMOR, M-OR-1, MOP, MOR, MOR1, OPRM opioid receptor, mu 1 C00042732
26577 PCOLCE2, PCPE2 procollagen C-endopeptidase enhancer 2 C00042732
5142 PDE4B, DPDE4, PDE4B5, PDEIVB phosphodiesterase 4B, cAMP-specific (EC:3.1.4.17) C00042732
5144 PDE4D, ACRDYS2, DPDE3, HSPDE4D, PDE43, PDE4DN2, STRK1 phosphodiesterase 4D, cAMP-specific (EC:3.1.4.17) C00042732
5146 PDE6C, ACHM5, COD4, PDEA2 phosphodiesterase 6C, cGMP-specific, cone, alpha prime (EC:3.1.4.35) C00042732
5173 PDYN, ADCA, PENKB, SCA23 prodynorphin C00042732
8061 FOSL1, FRA, FRA1, fra-1 FOS-like antigen 1 C00042226
5460 POU5F1, OCT3, OCT4, OTF-3, OTF3, OTF4, Oct-3, Oct-4 POU class 5 homeobox 1 C00042732
7799 PRDM2, HUMHOXY1, KMT8, MTB-ZF, RIZ, RIZ1, RIZ2 PR domain containing 2, with ZNF domain (EC:2.1.1.43) C00042732
5592 PRKG1, 1, AAT8, PKG, PRKG1B, PRKGR1B, cGK, cGK_1, cGK1, cGKI, cGKI-BETA, cGKI-alpha protein kinase, cGMP-dependent, type I (EC:2.7.11.12) C00042732
5617 PRL prolactin C00042732
128674 PROKR2, GPR73L1, GPR73b, GPRg2, HH3, KAL3, PKR2, dJ680N4.3 prokineticin receptor 2 C00042732
23362 PSD3, EFA6R, HCA67 pleckstrin and Sec7 domain containing 3 C00042732
5742 PTGS1, COX1, COX3, PCOX1, PES-1, PGG/HS, PGHS-1, PGHS1, PHS1, PTGHS prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00042732
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00042732
22913 RALY, HNRPCL2, P542 RALY heterogeneous nuclear ribonucleoprotein C00042732
9771 RAPGEF5, GFR, MR-GEF, REPAC Rap guanine nucleotide exchange factor (GEF) 5 C00042732
26575 RGS17, RGS-17, RGSZ2, hRGS17 regulator of G-protein signaling 17 C00042732
5104 SERPINA5, PAI-3, PAI3, PCI, PCI-B, PLANH3, PROCI serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 5 C00042732
137868 SGCZ, ZSG1 sarcoglycan, zeta C00042732
344558 SH3RF3, POSH2, SH3MD4 SH3 domain containing ring finger 3 C00042732
6571 SLC18A2, SVAT, SVMT, VAT2, VMAT2 solute carrier family 18 (vesicular monoamine transporter), member 2 C00042732
6518 SLC2A5, GLUT-5, GLUT5 solute carrier family 2 (facilitated glucose/fructose transporter), member 5 C00042732
6532 SLC6A4, 5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT, SERT1, hSERT solute carrier family 6 (neurotransmitter transporter), member 4 C00042732
6536 SLC6A9, GLYT1 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 C00042732
64754 SMYD3, KMT3E, ZMYND1, ZNFN3A1, bA74P14.1 SET and MYND domain containing 3 (EC:2.1.1.43) C00042732
6622 SNCA, NACP, PARK1, PARK4, PD1 synuclein, alpha (non A4 component of amyloid precursor) C00042732
6648 SOD2, IPOB, MNSOD, MVCD6 superoxide dismutase 2, mitochondrial (EC:1.15.1.1) C00042732
6855 SYP, MRXSYP synaptophysin C00042732
134864 TAAR1, RP11-295F4.9, TA1, TAR1, TRAR1 trace amine associated receptor 1 C00042732
7054 TH, DYT14, DYT5b, TYH tyrosine hydroxylase (EC:1.14.16.2) C00042732
7137 TNNI3, CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI troponin I type 3 (cardiac) C00042732
80036 TRPM3, GON-2, LTRPC3, MLSN2 transient receptor potential cation channel, subfamily M, member 3 C00042732
84196 USP48, RAP1GA1, USP31 ubiquitin specific peptidase 48 (EC:3.4.19.12) C00042732
79750 ZNF385D, ZNF659 zinc finger protein 385D C00042732

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#103780 Alcohol dependence P31645
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#300615 Brunner syndrome P21397
#212140 Carnitine deficiency, systemic primary; cdsp O76082
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959

KEGG DISEASE (7)

KEGG name UniProt
H00286 Crohn's disease O76082 (related)
H00525 Disorders of fatty-acid oxidation O76082 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00548 Brunner syndrome P21397 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H01171 Poor drug metabolism (PM) P33261 (related)

Diseases related to CTD interactions

240 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D015746 Abdominal Pain C00042226
C00042732
D000014 Abnormalities, Drug-Induced C00042226
C00042732
D054058 Acute Coronary Syndrome C00042226
C00042732
D015431 Weight Loss C00042226
C00042732
D014839 Vomiting C00042226
C00042732
D019969 Amphetamine-Related Disorders C00042226
C00042732
D018487 Ventricular Dysfunction, Left C00042226
C00042732
D020301 Vasospasm, Intracranial C00042226
C00042732
D000784 Aneurysm, Dissecting C00042226
C00042732
D017542 Aneurysm, Ruptured C00042226
C00042732
D000855 Anorexia C00042226
C00042732
D020293 Vasculitis, Central Nervous System C00042226
C00042732
D001008 Anxiety Disorders C00042226
C00042732
D014657 Vasculitis C00042226
C00042732
D001145 Arrhythmias, Cardiac C00042226
C00042732
D016055 Urinary Retention C00042226
C00042732
D013610 Tachycardia C00042226
C00042732
D001289 Attention Deficit Disorder with Hyperactivity C00042226
C00042732
D013375 Substance Withdrawal Syndrome C00042226
C00042732
D019966 Substance-Related Disorders C00042226
C00042732
D013345 Subarachnoid Hemorrhage C00042226
C00042732
D001925 Brain Damage, Chronic C00042226
C00042732
D001927 Brain Diseases C00042226
C00042732
D020521 Stroke C00042226
C00042732
D002545 Brain Ischemia C00042226
C00042732
D002012 Bruxism C00042226
C00042732
D019956 Stereotypic Movement Disorder C00042226
C00042732
D009202 Cardiomyopathies C00042226
C00042732
D002311 Cardiomyopathy, Dilated C00042226
C00042732
D013226 Status Epilepticus C00042226
C00042732
D012640 Seizures C00042226
C00042732
D002543 Cerebral Hemorrhage C00042226
C00042732
D002544 Cerebral Infarction C00042226
C00042732
D002637 Chest Pain C00042226
C00042732
D012559 Schizophrenia C00042226
C00042732
D002819 Chorea C00042226
C00042732
D012206 Rhabdomyolysis C00042226
C00042732
D019970 Cocaine-Related Disorders C00042226
C00042732
D003072 Cognition Disorders C00042226
C00042732
D017091 Colitis, Ischemic C00042226
C00042732
D011654 Pulmonary Edema C00042226
C00042732
D003329 Coronary Vasospasm C00042226
C00042732
D016757 Death, Sudden, Cardiac C00042226
C00042732
D003866 Depressive Disorder C00042226
C00042732
C536282 Pulmonary arterial hypertension C00042226
C00042732
D011618 Psychotic Disorders C00042226
C00042732
D004211 Disseminated Intravascular Coagulation C00042226
C00042732
D011605 Psychoses, Substance-Induced C00042226
C00042732
D064420 Drug-Related Side Effects and Adverse Reactions C00042226
C00042732
D004409 Dyskinesia, Drug-Induced C00042226
C00042732
D011595 Psychomotor Agitation C00042226
C00042732
D011297 Prenatal Exposure Delayed Effects C00042226
C00042732
D010300 Parkinson Disease C00042226
C00042732
D010259 Paranoid Disorders C00042226
C00042732
D009422 Nervous System Diseases C00042226
C00042732
D009410 Nerve Degeneration C00042226
C00042732
D009290 Narcolepsy C00042226
C00042732
D009212 Myoglobinuria C00042226
C00042732
D017202 Myocardial Ischemia C00042226
C00042732
D009203 Myocardial Infarction C00042226
C00042732
D009069 Movement Disorders C00042226
C00042732
D005334 Fever C00042226
C00042732
D005911 Gliosis C00042226
C00042732
D006130 Growth Disorders C00042226
C00042732
D006212 Hallucinations C00042226
C00042732
D001523 Mental Disorders C00042226
C00042732
D008569 Memory Disorders C00042226
C00042732
D007859 Learning Disorders C00042226
C00042732
D020300 Intracranial Hemorrhages C00042226
C00042732
D015658 HIV Infections C00042226
C00042732
D007174 Impulse Control Disorders C00042226
C00042732
D006930 Hyperalgesia C00042226
C00042732
D006948 Hyperkinesis C00042226
C00042732
D006973 Hypertension C00042226
C00042732
D006976 Hypertension, Pulmonary C00042226
C00042732
D007035 Hypothermia C00042226
C00042732
D010468 Perceptual Disorders C00042732
D018476 Hypokinesia C00042226
D020896 Hypovolemia C00042226
D016142 Holoprosencephaly C00042226
D020244 Infarction, Middle Cerebral Artery C00042226
D002532 Intracranial Aneurysm C00042226
D002542 Intracranial Embolism and Thrombosis C00042226
D006556 Heroin Dependence C00042226
D007673 Kidney Cortex Necrosis C00042226
D046649 Hematoma, Subdural, Spinal C00042226
D008107 Liver Diseases C00042226
D006341 Heart Rupture C00042226
D034381 Hearing Loss C00042226
D005221 Fatigue C00042226
D005119 Extravasation of Diagnostic and Therapeutic Materials C00042226
D004827 Epilepsy C00042226
D009205 Myocarditis C00042226
D004831 Epilepsies, Myoclonic C00042226
D004681 Encephalomyelitis, Autoimmune, Experimental C00042226
D009369 Neoplasms C00042226
D009395 Nephritis, Interstitial C00042226
D004438 Ecchymosis C00042226
D001068 Eating Disorders C00042226
D019150 Neuroaxonal Dystrophies C00042226
D019636 Neurodegenerative Diseases C00042226
D009459 Neuroleptic Malignant Syndrome C00042226
D010146 Pain C00042226
D004421 Dystonia C00042226
D010291 Paresis C00042226
D019263 Dysthymic Disorder C00042226
D010493 Pericarditis C00042226
D010554 Personality Disorders C00042226
D017689 Polydactyly C00042226
D011230 Precancerous Conditions C00042226
D011248 Pregnancy Complications C00042226
D047928 Premature Birth C00042226
D004417 Dyspnea C00042226
D011317 Priapism C00042226
D020820 Dyskinesias C00042226
D062787 Drug Overdose C00042226
D004195 Disease Models, Animal C00042226
D002658 Developmental Disabilities C00042226
D003323 Coronary Aneurysm C00042226
D011693 Purpura C00042226
D011782 Quadriplegia C00042226
D012128 Respiratory Distress Syndrome, Adult C00042226
C535485 Chromosome 13q trisomy C00042226
D002653 Child Behavior Disorders C00042226
D002385 Cataplexy C00042226
D012652 Self Mutilation C00042226
D020018 Sexual Dysfunctions, Psychological C00042226
D012893 Sleep Disorders C00042226
D002340 Carotid Artery Diseases C00042226
D006502 Budd-Chiari Syndrome C00042226
D001930 Brain Injuries C00042226
D053608 Stupor C00042226
D001919 Bradycardia C00042226
D001832 Body Temperature Changes C00042226
D001714 Bipolar Disorder C00042226
D001284 Atrophy C00042226
D054549 Takotsubo Cardiomyopathy C00042226
D001167 Arteritis C00042226
D017545 Aortic Aneurysm, Thoracic C00042226
D056988 Anterior Wall Myocardial Infarction C00042226
D000783 Aneurysm C00042226
D000740 Anemia C00042226
D000647 Amnesia C00042226
D058186 Acute Kidney Injury C00042226
D000037 Abruptio Placentae C00042732
D000379 Agoraphobia C00042732
D015526 AIDS Dementia Complex C00042732
D000437 Alcoholism C00042732
D000789 Angina, Unstable C00042732
D050197 Atherosclerosis C00042732
D001264 Athetosis C00042732
D054537 Atrioventricular Block C00042732
D053099 Azotemia C00042732
D001480 Basal Ganglia Diseases C00042732
D006332 Cardiomegaly C00042732
D002318 Cardiovascular Diseases C00042732
D002375 Catalepsy C00042732
D002386 Cataract C00042732
D002493 Central Nervous System Diseases C00042732
D002561 Cerebrovascular Disorders C00042732
D023341 Chills C00042732
D002779 Cholestasis C00042732
D019955 Conduct Disorder C00042732
D003244 Consciousness Disorders C00042732
D003320 Corneal Ulcer C00042732
D003693 Delirium C00042732
D003731 Dental Caries C00042732
D003865 Depressive Disorder, Major C00042732
D004244 Dizziness C00042732
D004342 Drug Hypersensitivity C00042732
D004401 Dysarthria C00042732
D004487 Edema C00042732
D009877 Endophthalmitis C00042732
D004802 Eosinophilia C00042732
D004830 Epilepsy, Tonic-Clonic C00042732
D005317 Fetal Growth Retardation C00042732
D020233 Gait Disorders, Neurologic C00042732
D005767 Gastrointestinal Diseases C00042732
D006261 Headache C00042732
D006331 Heart Diseases C00042732
D006333 Heart Failure C00042732
D006606 Hiccup C00042732
D006967 Hypersensitivity C00042732
D006984 Hypertrophy C00042732
D017379 Hypertrophy, Left Ventricular C00042732
D007154 Immune System Diseases C00042732
D007676 Kidney Failure, Chronic C00042732
D007683 Kidney Tubular Necrosis, Acute C00042732
D056784 Leukoencephalopathies C00042732
D017114 Liver Failure, Acute C00042732
D008171 Lung Diseases C00042732
D020422 Mononeuropathies C00042732
D019964 Mood Disorders C00042732
D016472 Motor Neuron Disease C00042732
D019957 Motor Skills Disorders C00042732
D009059 Mouth Diseases C00042732
D009127 Muscle Rigidity C00042732
D009325 Nausea C00042732
D009336 Necrosis C00042732
D019954 Neurobehavioral Manifestations C00042732
D020258 Neurotoxicity Syndromes C00042732
D009771 Obsessive-Compulsive Disorder C00042732
D009784 Occupational Diseases C00042732
D009901 Optic Nerve Diseases C00042732
D010024 Osteoporosis C00042732
D016584 Panic Disorder C00042732
D010202 Panophthalmitis C00042732
D010254 Paranasal Sinus Diseases C00042732
D010292 Paresthesia C00042732
D010302 Parkinson Disease, Secondary C00042732
D007022 Hypotension C00042226
D016491 Peripheral Vascular Diseases C00042732
D011041 Poisoning C00042732
D049188 Prenatal Injuries C00042732
D011596 Psychomotor Disorders C00042732
D051437 Renal Insufficiency C00042732
D012140 Respiratory Tract Diseases C00042732
D012164 Retinal Diseases C00042732
D015423 Scleritis C00042732
D012749 Sexually Transmitted Diseases C00042732
D012769 Shock C00042732
D012770 Shock, Cardiogenic C00042732
D012871 Skin Diseases C00042732
D007319 Sleep Initiation and Maintenance Disorders C00042732
D018461 Soft Tissue Infections C00042732
D013064 Speech Disorders C00042732
D013207 Staphylococcal Skin Infections C00042732
D015819 Substance Abuse, Intravenous C00042732
D013587 Syphilis C00042732
D013617 Tachycardia, Supraventricular C00042732
D017180 Tachycardia, Ventricular C00042732
D013706 Temporomandibular Joint Dysfunction Syndrome C00042732
D014076 Tooth Diseases C00042732
D014202 Tremor C00042732
D014313 Trismus C00042732
D018754 Ventricular Dysfunction C00042732
D014693 Ventricular Fibrillation C00042732
D018879 Ventricular Premature Complexes C00042732
D014786 Vision Disorders C00042732
D014987 Xerostomia C00042732