Species

KNApSAcK Entry

Organism name Meriandra benghalensis
Genus Meriandra
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Meriandra
Linked NCBI taxonomy ID 392635
Linked level genus

Family

Family in NCBI taxonomy Lamiaceae
ID 4136

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (8)

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
C00004603 External link 512 Penduletin
/ 5,4'-Dihydroxy-3,6,7-trimethoxyflavone
/ 5-Hydroxy-2-(4-hydroxyphenyl)-3,6,7-trimethoxy-4H-1-benzopyran-4-one
CHEMBL165509
3 / 3 / 0 No. 3 No. 15
C00030742 External link 512 Maslinic acid
/ Crategolic acid
/ 2alpha,3beta-Dihydroxyolean-12-en-28-oic acid
CHEMBL201515
CHEMBL383749
CHEMBL482673
CHEMBL577380
C412811
8 / 5 / 4 No. 13 No. 51
C00019064 External link 512 Oleanolic acid
/ Astrantiagenin C
/ Virgaureagenin B
/ 3beta-Hydroxyolean-12-en-28-oic acid
CHEMBL56615
CHEMBL168
CHEMBL180553
CHEMBL365375
CHEMBL486382
CHEMBL1413646
CHEMBL1436454
D009828
30 / 8 / 12 21 / 15 No. 13 No. 51
C00029633 External link 512 Ursolic acid
/ Acetylursolic acid
CHEMBL55086
CHEMBL410525
4 / 2 / 2 No. 177
C00017525 External link 512 Benghalensitriol
No. 1209
C00000819 External link 512 (+)-Camphor
CHEMBL504760
CHEMBL1316134
D002164
99 / 56 / 51 5 / 3 No. 1921 No. 35
C00012683 External link 512 Benghalensin A
/ [6aS-(6aalpha,9alpha,9aalpha)]-3,6a,7,8,9,9a-Hexahydro-9a-hydroxy-6a-methyl-9-(1-methylethyl)-4H-naphtho[1,8-cd]-1,2-dioxin-4-one
No. 4293
C00012684 External link 512 Benghalensin B
/ (-)-Benghalensin B
/ [5aS-(5aalpha,8beta,8aalpha)]-2,5a,6,7,8,8a-Hexahydro-8,8a-dihydroxy-5a-methyl-8-(1-methylethyl)-3H-naphtho[1,8-bc]furan-3-one
No. 4293

Human Protein / Gene in interactions

129 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P15121 Aldose reductase Enzyme C00004603 C00019064 C00030742 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00000819 C00019064 0 / 0
P17706 Tyrosine-protein phosphatase non-receptor type 2 Tyr C00019064 C00030742 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00019064 C00029633 0 / 0
O60218 Aldo-keto reductase family 1 member B10 Enzyme C00019064 C00030742 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000819 C00019064 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000819 C00019064 0 / 3
P29350 Tyrosine-protein phosphatase non-receptor type 6 Tyr C00019064 C00030742 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00019064 C00029633 2 / 2
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00019064 C00030742 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000819 C00019064 0 / 0
P06746 DNA polymerase beta Enzyme C00019064 C00029633 0 / 0
P10586 Receptor-type tyrosine-protein phosphatase F Receptor tyrosine-protein phosphatase C00019064 C00030742 0 / 0
Q06124 Tyrosine-protein phosphatase non-receptor type 11 Tyr C00019064 C00030742 4 / 2
P03372 Estrogen receptor NR3A1 C00000819 1 / 1
P17252 Protein kinase C alpha type Alpha C00000819 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00000819 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00000819 2 / 2
P24666 Low molecular weight phosphotyrosine protein phosphatase Tyr C00019064 0 / 0
Q8TDU6 G-protein coupled bile acid receptor 1 Steroid-like ligand receptor C00019064 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00019064 0 / 0
P02545 Prelamin-A/C Unclassified protein C00000819 11 / 10
P00918 Carbonic anhydrase 2 Lyase C00000819 1 / 2
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00000819 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00000819 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00000819 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00000819 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00000819 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00000819 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00000819 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00000819 0 / 0
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00019064 0 / 0
P08183 Multidrug resistance protein 1 drug C00004603 1 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00000819 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00000819 0 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00000819 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00000819 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000819 0 / 1
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00000819 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00000819 2 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00000819 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00000819 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00000819 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00000819 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00000819 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00000819 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00000819 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00000819 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00000819 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000819 0 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00000819 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00019064 0 / 0
O75496 Geminin Unclassified protein C00019064 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00000819 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00000819 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00000819 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00000819 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00000819 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00000819 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00000819 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00000819 0 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00000819 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00000819 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00000819 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00000819 1 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00019064 0 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00000819 0 / 0
P08311 Cathepsin G S1A C00000819 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00000819 1 / 0
P03956 Interstitial collagenase M10A C00000819 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00000819 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00019064 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00000819 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00000819 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00000819 0 / 0
P08246 Neutrophil elastase S1A C00000819 2 / 1
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00000819 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00000819 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00000819 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00000819 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00000819 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00000819 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00000819 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00000819 0 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00000819 2 / 2
P18433 Receptor-type tyrosine-protein phosphatase alpha Receptor tyrosine-protein phosphatase C00019064 0 / 0
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr C00019064 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00000819 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000819 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00000819 2 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000819 0 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00004603 2 / 0
O75762 Transient receptor potential cation channel subfamily A member 1 Unclassified protein C00000819 1 / 0
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00000819 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00000819 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00000819 0 / 0
P29466 Caspase-1 C14 C00000819 0 / 0
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00000819 1 / 0
P22303 Acetylcholinesterase Hydrolase C00000819 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00000819 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00000819 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00000819 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00000819 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00000819 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00000819 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00000819 0 / 0
P35228 Nitric oxide synthase, inducible Enzyme C00019064 1 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000819 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000819 0 / 1
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00000819 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00019064 0 / 0
Q8NET8 Transient receptor potential cation channel subfamily V member 3 Unclassified protein C00000819 1 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000819 4 / 3
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00000819 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00000819 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00000819 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00000819 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00000819 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00000819 0 / 1
P11217 Glycogen phosphorylase, muscle form Enzyme C00030742 1 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00000819 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000819 1 / 0
P04054 Phospholipase A2 Enzyme C00019064 0 / 0
P23469 Receptor-type tyrosine-protein phosphatase epsilon Receptor tyrosine-protein phosphatase C00019064 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00029633 0 / 0
O00255 Menin Unclassified protein C00000819 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000819 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00019064 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00019064 1 / 4

26 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1555 CYP2B6, CPB6, CYP2B, CYP2B7, CYP2B7P, CYPIIB6, EFVM, IIB1, P450 cytochrome P450, family 2, subfamily B, polypeptide 6 (EC:1.14.14.1) C00000819
2554 GABRA1, ECA4, EJM, EJM5 gamma-aminobutyric acid (GABA) A receptor, alpha 1 C00000819
2561 GABRB2 gamma-aminobutyric acid (GABA) A receptor, beta 2 C00000819
2566 GABRG2, CAE2, ECA2, GEFSP3 gamma-aminobutyric acid (GABA) A receptor, gamma 2 C00000819
162514 TRPV3, OLMS, VRL3 transient receptor potential cation channel, subfamily V, member 3 C00000819
177 AGER, RAGE advanced glycosylation end product-specific receptor C00019064
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00019064
841 CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) C00019064
847 CAT catalase (EC:1.11.1.6) C00019064
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00019064
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00019064
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) C00019064
3065 HDAC1, GON-10, HD1, RPD3, RPD3L1 histone deacetylase 1 (EC:3.5.1.98) C00019064
3146 HMGB1, HMG1, HMG3, SBP-1 high mobility group box 1 C00019064
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00019064
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00019064
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) C00019064
4233 MET, AUTS9, HGFR, RCCP2, c-Met met proto-oncogene (EC:2.7.10.1) C00019064
4780 NFE2L2, NRF2 nuclear factor, erythroid 2-like 2 C00019064
5052 PRDX1, MSP23, NKEF-A, NKEFA, PAG, PAGA, PAGB, PRX1, PRXI, TDPX2 peroxiredoxin 1 (EC:1.11.1.15) C00019064
5728 PTEN, 10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC1, PTEN1, TEP1 phosphatase and tensin homolog (EC:3.1.3.67 3.1.3.16 3.1.3.48) C00019064
6401 SELE, CD62E, ELAM, ELAM1, ESEL, LECAM2 selectin E C00019064
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00019064
7150 TOP1, TOPI topoisomerase (DNA) I (EC:5.99.1.2) C00019064
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00019064
7412 VCAM1, CD106, INCAM-100 vascular cell adhesion molecule 1 C00019064

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (68)

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
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#614490 Blood group, junior system; jr Q9UNQ0
#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
#615040 Episodic pain syndrome, familial, 1; feps1 O75762
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#137800 Glioma susceptibility 1; glm1 P04626
#232600 Glycogen storage disease v P11217
#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
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#612244 Inflammatory bowel disease 13; ibd13 P08183
#603932 Intervertebral disc disease; idd P14780
#607785 Juvenile myelomonocytic leukemia; jmml Q06124
#151100 Leopard syndrome 1 Q06124
#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
#611162 Malaria, susceptibility to P35228
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
%300852 Mental retardation, x-linked 88; mrx88 P50052
#156250 Metachondromatosis; metcds Q06124
#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
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#163950 Noonan syndrome 1; ns1 Q06124
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#614594 Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques Q8NET8
#260540 Parkinson-dementia syndrome P10636
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#190300 Tremor, hereditary essential, 1; etm1 P35462
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#610379 West nile virus, susceptibility to P51681
#112100 Yt blood group antigen P22303

KEGG DISEASE (59)

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)
P35228 (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)
P11511 (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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00069 Glycogen storage diseases (GSD) P11217 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00408 Type I diabetes mellitus P17706 (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)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00523 Noonan syndrome and related disorders Q06124 (related)
H01018 Metachondromatosis Q06124 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)

Diseases related to CTD interactions

18 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003371 Cough C00000819
D004487 Edema C00000819
D012640 Seizures C00000819
D002252 Carbon Tetrachloride Poisoning C00019064
D056486 Drug-Induced Liver Injury C00019064
D050171 Dyslipidemias C00019064
D018149 Glucose Intolerance C00019064
D006949 Hyperlipidemias C00019064
D007249 Inflammation C00019064
D007674 Kidney Diseases C00019064
D008103 Liver Cirrhosis C00019064
D008106 Liver Cirrhosis, Experimental C00019064
D008107 Liver Diseases C00019064
D017202 Myocardial Ischemia C00019064
D009369 Neoplasms C00019064
D009765 Obesity C00019064
D011041 Poisoning C00019064
D011230 Precancerous Conditions C00019064