Species

KNApSAcK Entry

Organism name Uvaria mocali
Genus Uvaria
Family Annonaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Uvaria
Linked NCBI taxonomy ID 174969
Linked level genus

Family

Family in NCBI taxonomy Annonaceae
ID 22140

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Magnoliophyta
ID 3398

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
C00008158 External link 512 5,7,8-Trimethoxyflavanone
No. 25 No. 14
C00025935 External link 512 Lysicamine
/ Oxonuciferine
CHEMBL510090
C069090
No. 74
C00001878 External link 512 Liriodenine
/ Oxoushinsunine
/ Spermatheridine
CHEMBL37736
C026980
5 / 3 / 1 No. 74
C00027145 External link 512 Isomoschatoline
No. 74
C00048940 External link 512 2'-Hydroxy-4',5',6'-trimethoxychalcone
No. 79
C00048941 External link 512 2'-Hydroxy-4',6'-dimethoxychalcone
CHEMBL104255
19 / 31 / 55 No. 79
C00014606 External link 512 2-Hydroxy-4,5,6-trimethoxydihydrochalcone
No. 90 No. 13
C00000207 External link 512 Benzoic acid
CHEMBL541
D019817
97 / 39 / 33 24 / 1 No. 2192

Human Protein / Gene in interactions

120 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000207 C00048941 0 / 1
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00000207 2 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00048941 0 / 0
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00000207 0 / 0
Q99700 Ataxin-2 Unclassified protein C00048941 1 / 1
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
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00000207 0 / 0
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
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00048941 1 / 4
Q99489 D-aspartate oxidase Enzyme C00000207 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00000207 3 / 2
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
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
P30926 Neuronal acetylcholine receptor subunit beta-4 CHRN beta C00001878 0 / 0
P32297 Neuronal acetylcholine receptor subunit alpha-3 CHRN alpha C00001878 1 / 0
P17787 Neuronal acetylcholine receptor subunit beta-2 CHRN beta C00001878 1 / 1
P43681 Neuronal acetylcholine receptor subunit alpha-4 CHRN alpha C00001878 1 / 1
P14920 D-amino-acid oxidase Enzyme C00000207 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00000207 1 / 8
P11473 Vitamin D3 receptor NR1I1 C00048941 2 / 3
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
Q14761 Protein tyrosine phosphatase receptor type C-associated protein Enzyme C00001878 0 / 0
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00000207 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00000207 1 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00000207 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00048941 2 / 0
O75496 Geminin Unclassified protein C00048941 0 / 0
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
Q92731 Estrogen receptor beta NR3A2 C00000207 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00000207 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
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00048941 0 / 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
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00048941 7 / 3
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00048941 1 / 2
P11021 78 kDa glucose-regulated protein Unclassified protein C00048941 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00048941 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
P04637 Cellular tumor antigen p53 Transcription Factor C00048941 7 / 37
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000207 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00048941 3 / 3
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00048941 2 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00048941 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00000207 0 / 0
P03372 Estrogen receptor NR3A1 C00000207 1 / 1
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
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000207 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000207 1 / 0
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00000207 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00048941 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00048941 4 / 3
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
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00048941 1 / 0

24 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
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
2729 GCLC, GCL, GCS, GLCL, GLCLC glutamate-cysteine ligase, catalytic subunit (EC:6.3.2.2) C00000207
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
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) 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 (71)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103780 Alcohol dependence P08172
P14416
P31645
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#208900 Ataxia-telangiectasia; at Q13315
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#614490 Blood group, junior system; jr Q9UNQ0
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#300615 Brunner syndrome P21397
#114500 Colorectal cancer; crc P84022
#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
#600513 Epilepsy, nocturnal frontal lobe, 1; enfl1 P43681
#605375 Epilepsy, nocturnal frontal lobe, 3; enfl3 P17787
#133239 Esophageal cancer P04637
#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 O75874
P04626
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#603932 Intervertebral disc disease; idd P14780
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04626
P04637
#608516 Major depressive disorder; mdd P08172
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
%300852 Mental retardation, x-linked 88; mrx88 P50052
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#126200 Multiple sclerosis, susceptibility to; ms P08575
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#159900 Myoclonic dystonia P14416
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#607276 Resting heart rate, variation in P08588
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#612052 Smoking as a quantitative trait locus 3; sqtl3 P32297
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#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
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#610379 West nile virus, susceptibility to P51681
#112100 Yt blood group antigen P22303

KEGG DISEASE (74)

KEGG name UniProt
H00016 Oral cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P00533 (related)
P04637 (related)
P04637 (marker)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
P04637 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
P04637 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
P04637 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00026 Endometrial Cancer P03372 (marker)
P04626 (related)
P04637 (related)
Q92731 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00019 Pancreatic cancer P04626 (related)
P04637 (related)
P04637 (marker)
H00027 Ovarian cancer P04626 (related)
P04637 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
P04637 (related)
H00046 Cholangiocarcinoma P04626 (related)
P04637 (related)
P35354 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
Q13315 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
P14780 (related)
P35354 (related)
H00029 Vulvar cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00044 Cancer of the anal canal P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00807 Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) P17787 (related)
P43681 (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)
Q99714 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (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)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (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

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003877 Dermatitis, Contact C00000207