Species

KNApSAcK Entry

Organism name Paeonia hybrida
Genus Paeonia
Family Paeoniaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Paeonia
Linked NCBI taxonomy ID 13625
Linked level genus

Family

Family in NCBI taxonomy Paeoniaceae
ID 24943

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (9)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00034096 External link 512 Paeonovicinoside
/ (-)-Paeonovicinoside
No. 930
C00032987 External link 512 Galloylpaeoniflorin
CHEMBL1077642
No. 1069
C00002682 External link 512 Vanillic acid
/ 3-Methoxy-4-hydroxybenzoic acid
CHEMBL120568
D014641
5 / 3 / 3 5 / 0 No. 1073
C00033623 External link 512 Albiflorin
CHEMBL1939883
C014959
1 / 1 / 1 No. 1566
C00003011 External link 512 Paeoniflorin
CHEMBL1078549
CHEMBL1397567
CHEMBL1972762
C015423
4 / 4 / 8 3 / 2 No. 1566
C00011060 External link 512 Lactiflorin
No. 1566
C00030754 External link 512 Methyl gallate
/ Methyl 3,4,5-trihydroxybenzoate
CHEMBL65675
C052082
16 / 15 / 13 No. 1722
C00000207 External link 512 Benzoic acid
CHEMBL541
D019817
97 / 39 / 33 24 / 1 No. 2192
C00010954 External link 512 Paeoniflorigenone
/ (+)-Paeoniflorigenone
CHEMBL1077668
C042713
No. 5422

Human Protein / Gene in interactions

120 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P03372 Estrogen receptor NR3A1 C00000207 C00002682 C00003011 C00033623 1 / 1
Q92731 Estrogen receptor beta NR3A2 C00000207 0 / 1
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00000207 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00000207 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000207 0 / 3
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00000207 2 / 2
P08246 Neutrophil elastase S1A C00000207 2 / 1
P33765 Adenosine receptor A3 Adenosine receptor C00000207 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00000207 0 / 0
P06746 DNA polymerase beta Enzyme C00030754 0 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00000207 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00030754 1 / 1
P29466 Caspase-1 C14 C00000207 0 / 0
P17252 Protein kinase C alpha type Alpha C00000207 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00000207 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00000207 2 / 2
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00030754 0 / 0
Q99489 D-aspartate oxidase Enzyme C00000207 0 / 0
P02545 Prelamin-A/C Unclassified protein C00030754 11 / 10
P55789 FAD-linked sulfhydryl oxidase ALR Enzyme C00030754 1 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00000207 3 / 2
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00030754 1 / 1
P00918 Carbonic anhydrase 2 Lyase C00000207 1 / 2
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00000207 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00000207 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00000207 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00000207 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00000207 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00000207 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00000207 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00000207 0 / 0
P02768 Serum albumin Secreted protein C00030754 0 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00000207 0 / 0
Q9UQ49 Sialidase-3 Enzyme C00000207 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00000207 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00000207 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000207 0 / 1
P14920 D-amino-acid oxidase Enzyme C00000207 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00000207 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00000207 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000207 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00000207 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00000207 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00000207 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00000207 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00000207 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00000207 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00000207 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00000207 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00003011 0 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00000207 0 / 0
P39748 Flap endonuclease 1 Enzyme C00030754 0 / 0
P42858 Huntingtin Unclassified protein C00002682 1 / 1
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00000207 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00000207 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00000207 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00000207 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00000207 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00000207 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00000207 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00030754 0 / 0
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00000207 0 / 0
P15121 Aldose reductase Enzyme C00002682 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00000207 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00000207 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00000207 1 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00000207 0 / 0
P08311 Cathepsin G S1A C00000207 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00000207 1 / 0
P03956 Interstitial collagenase M10A C00000207 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00000207 0 / 0
Q9GZT4 Serine racemase Enzyme C00000207 0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00030754 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00030754 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00000207 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00000207 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00000207 0 / 0
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00000207 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00000207 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00000207 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00000207 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00000207 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00000207 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00000207 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00000207 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00000207 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000207 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00000207 2 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000207 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00000207 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000207 1 / 0
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00000207 1 / 0
P22303 Acetylcholinesterase Hydrolase C00000207 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00000207 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00000207 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00000207 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00000207 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00000207 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00000207 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00000207 0 / 0
P51580 Thiopurine S-methyltransferase Enzyme C00002682 1 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000207 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000207 0 / 1
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00000207 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002682 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00030754 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00030754 0 / 0
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00000207 0 / 0
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00000207 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00000207 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00000207 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00000207 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00000207 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00000207 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00000207 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00030754 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00030754 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00030754 1 / 1
O00255 Menin Unclassified protein C00003011 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003011 1 / 2

31 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00000207 C00002682
2729 GCLC, GCL, GCS, GLCL, GLCLC glutamate-cysteine ligase, catalytic subunit (EC:6.3.2.2) C00000207
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00003011
664 BNIP3, NIP3 BCL2/adenovirus E1B 19kDa interacting protein 3 C00003011
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002682
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00002682
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002682
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) C00002682
231 AKR1B1, ADR, ALDR1, ALR2, AR aldo-keto reductase family 1, member B1 (aldose reductase) (EC:1.1.1.21) C00000207
57016 AKR1B10, AKR1B11, AKR1B12, ALDRLn, ARL-1, ARL1, HIS, HSI aldo-keto reductase family 1, member B10 (aldose reductase) (EC:1.1.1.2) C00000207
1645 AKR1C1, 2-ALPHA-HSD, 20-ALPHA-HSD, C9, DD1, DD1/DD2, DDH, DDH1, H-37, HAKRC, HBAB, MBAB aldo-keto reductase family 1, member C1 (EC:1.3.1.20 1.1.1.149 1.1.1.112) C00000207
8644 AKR1C3, DD3, DDX, HA1753, HAKRB, HAKRe, HSD17B5, PGFS, hluPGFS aldo-keto reductase family 1, member C3 (EC:1.3.1.20 1.1.1.188 1.1.1.239 1.1.1.64 1.1.1.112 1.1.1.357) C00000207
2235 FECH, EPP, FCE ferrochelatase (EC:4.99.1.1) C00000207
2512 FTL, NBIA3 ferritin, light polypeptide C00000207
2539 G6PD, G6PD1 glucose-6-phosphate dehydrogenase (EC:1.1.1.49) C00000207
3091 HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) C00003011
2730 GCLM, GLCLR glutamate-cysteine ligase, modifier subunit (EC:6.3.2.2) C00000207
2936 GSR glutathione reductase (EC:1.8.1.7) C00000207
2938 GSTA1, GST2, GSTA1-1, GTH1 glutathione S-transferase alpha 1 (EC:2.5.1.18) C00000207
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00000207
4097 MAFG, hMAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog G C00000207
4199 ME1, HUMNDME, MES malic enzyme 1, NADP(+)-dependent, cytosolic (EC:1.1.1.40) C00000207
4489 MT1A, MT1, MT1S, MTC metallothionein 1A C00000207
4502 MT2A, MT2 metallothionein 2A C00000207
1728 NQO1, DHQU, DIA4, DTD, NMOR1, NMORI, QR1 NAD(P)H dehydrogenase, quinone 1 (EC:1.6.5.2) C00000207
5226 PGD, 6PGD phosphogluconate dehydrogenase (EC:1.1.1.44) C00000207
22949 PTGR1, LTB4DH, PGR1, ZADH3 prostaglandin reductase 1 (EC:1.3.1.48 1.3.1.74) C00000207
6566 SLC16A1, HHF7, MCT, MCT1 solute carrier family 16 (monocarboxylate transporter), member 1 C00000207
140809 SRXN1, C20orf139, Npn3, SRX, SRX1 sulfiredoxin 1 (EC:1.8.98.2) C00000207
7295 TXN, TRDX, TRX, TRX1 thioredoxin C00000207
7296 TXNRD1, GRIM-12, TR, TR1, TRXR1, TXNR thioredoxin reductase 1 (EC:1.8.1.9) C00000207

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (59)

OMIM preferred title UniProt
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#103780 Alcohol dependence P08172
P14416
P31645
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#162800 Cyclic neutropenia P08246
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#615363 Estrogen resistance; estrr P03372
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#137800 Glioma susceptibility 1; glm1 P04626
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#603932 Intervertebral disc disease; idd P14780
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04626
#608516 Major depressive disorder; mdd P08172
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
%300852 Mental retardation, x-linked 88; mrx88 P50052
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#126200 Multiple sclerosis, susceptibility to; ms P08575
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#159900 Myoclonic dystonia P14416
#613076 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay P55789
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#607276 Resting heart rate, variation in P08588
#275210 Restrictive dermopathy, lethal P02545
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#610460 Thiopurine s-methyltransferase deficiency P51580
#190300 Tremor, hereditary essential, 1; etm1 P35462
#610379 West nile virus, susceptibility to P51681
#278300 Xanthinuria, type i P47989
#112100 Yt blood group antigen P22303

KEGG DISEASE (55)

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)
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00026 Endometrial Cancer P03372 (marker)
P04626 (related)
Q92731 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00019 Pancreatic cancer P04626 (related)
H00027 Ovarian cancer P04626 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
H00046 Cholangiocarcinoma P04626 (related)
P35354 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H01205 Coumarin resistance P11712 (related)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00548 Brunner syndrome P21397 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00192 Xanthinuria P47989 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
H00964 Thiopurine S-methyltransferase deficiency (TPMT deficiency) P51580 (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)
H00725 Short QT syndrome Q12809 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000647 Amnesia C00003011
D007022 Hypotension C00003011
D003877 Dermatitis, Contact C00000207