Species

KNApSAcK Entry

Organism name Penicillium brevicompactum
Genus Penicillium
Family Trichocomaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Penicillium brevicompactum
Linked NCBI taxonomy ID 5074
Linked level species

Family

Family in NCBI taxonomy Aspergillaceae
ID 1131492

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Fungi
ID 4751

Plant class

Plant class
ID

Metabolite list (11)

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
C00042430 External link 512 cyclo(D-Leu-L-Trp)
CHEMBL365348
CHEMBL471388
1 / 0 / 0 No. 1509
C00042429 External link 512 cyclo(D-Ile-L-Trp)
CHEMBL472229
No. 1509
C00011280 External link 512 Brevianamide F
/ L-Prolyl-L-tryptophan anhydride
CHEMBL563557
CHEMBL2031508
CHEMBL2031509
CHEMBL2031510
No. 1509
C00042302 External link 512 Brevicompanine C
/ (-)-Brevicompanine C
CHEMBL472025
No. 3186
C00027029 External link 512 Brevicompanine B
/ (-)-Brevicompanine B
No. 3186
C00027028 External link 512 Brevicompanine A
/ (-)-Brevicompanine A
No. 3186
C00011278 External link 512 Brevianamide C
No. 4759
C00011279 External link 512 Brevianamide D
No. 4759
C00018753 External link 512 MPA
/ Melbex
/ NSC 129185
/ Lilly 68618
/ Mycophenolic acid
CHEMBL866
D009173
111 / 72 / 58 29 / 11 No. 5526
C00026932 External link 512 Brevianamide E
No. 6081
C00027956 External link 512 Brevioxime
/ (-)-Brevioxime
No. 8874

Human Protein / Gene in interactions

112 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00018753 1 / 0
Q16637 Survival motor neuron protein Unclassified protein C00018753 4 / 1
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00018753 0 / 0
P20839 Inosine-5'-monophosphate dehydrogenase 1 Oxidoreductase C00018753 2 / 2
P21728 D(1A) dopamine receptor Dopamine receptor C00018753 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00018753 0 / 3
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00018753 2 / 2
P08246 Neutrophil elastase S1A C00018753 2 / 1
P33765 Adenosine receptor A3 Adenosine receptor C00018753 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00018753 0 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00018753 0 / 0
P29466 Caspase-1 C14 C00018753 0 / 0
P17252 Protein kinase C alpha type Alpha C00018753 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00018753 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00018753 2 / 2
P02545 Prelamin-A/C Unclassified protein C00018753 11 / 10
P37840 Alpha-synuclein Unclassified protein C00018753 4 / 2
P12268 Inosine-5'-monophosphate dehydrogenase 2 Oxidoreductase C00018753 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00018753 1 / 2
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00018753 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00018753 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00018753 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00018753 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00018753 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00018753 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00018753 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00018753 0 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00018753 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00018753 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00018753 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00018753 0 / 1
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00018753 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00018753 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00018753 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00018753 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00018753 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00018753 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00018753 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00018753 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00018753 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00018753 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00018753 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00018753 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00018753 0 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00018753 0 / 0
O75496 Geminin Unclassified protein C00018753 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00018753 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00018753 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00018753 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00018753 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00018753 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00018753 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00018753 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00018753 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00018753 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00018753 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00018753 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00018753 1 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00018753 0 / 0
P08311 Cathepsin G S1A C00018753 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00018753 1 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00018753 0 / 0
P07384 Calpain-1 catalytic subunit C2 C00042430 0 / 0
P03956 Interstitial collagenase M10A C00018753 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00018753 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00018753 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00018753 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00018753 0 / 0
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00018753 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00018753 2 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00018753 5 / 3
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00018753 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00018753 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00018753 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00018753 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00018753 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00018753 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00018753 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00018753 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00018753 2 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00018753 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00018753 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00018753 2 / 2
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00018753 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00018753 0 / 0
P03372 Estrogen receptor NR3A1 C00018753 1 / 1
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00018753 1 / 0
P22303 Acetylcholinesterase Hydrolase C00018753 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00018753 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00018753 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00018753 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00018753 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00018753 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00018753 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00018753 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00018753 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00018753 0 / 1
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00018753 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00018753 5 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00018753 0 / 0
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00018753 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00018753 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00018753 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00018753 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00018753 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00018753 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00018753 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00018753 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00018753 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00018753 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00018753 1 / 4
Q13148 TAR DNA-binding protein 43 Unclassified protein C00018753 1 / 1

29 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00018753
466 ATF1, EWS-ATF1, FUS/ATF-1, TREB36 activating transcription factor 1 C00018753
581 BAX, BCL2L4 BCL2-associated X protein C00018753
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00018753
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00018753
1027 CDKN1B, CDKN4, KIP1, MEN1B, MEN4, P27KIP1 cyclin-dependent kinase inhibitor 1B (p27, Kip1) C00018753
1385 CREB1, CREB cAMP responsive element binding protein 1 C00018753
1558 CYP2C8, CPC8, CYPIIC8, MP-12/MP-20 cytochrome P450, family 2, subfamily C, polypeptide 8 (EC:1.14.14.1) C00018753
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) C00018753
1577 CYP3A5, CP35, CYPIIIA5, P450PCN3, PCN3 cytochrome P450, family 3, subfamily A, polypeptide 5 (EC:1.14.14.1) C00018753
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00018753
2932 GSK3B glycogen synthase kinase 3 beta (EC:2.7.11.1 2.7.11.26) C00018753
3558 IL2, IL-2, TCGF, lymphokine interleukin 2 C00018753
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00018753
22914 KLRK1, CD314, D12S2489E, KLR, NKG2-D, NKG2D killer cell lectin-like receptor subfamily K, member 1 C00018753
4067 LYN, JTK8, p53Lyn, p56Lyn v-yes-1 Yamaguchi sarcoma viral related oncogene homolog (EC:2.7.10.2) C00018753
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00018753
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) C00018753
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00018753
5601 MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK mitogen-activated protein kinase 9 (EC:2.7.11.24) C00018753
4137 MAPT, DDPAC, FTDP-17, MAPTL, MSTD, MTBT1, MTBT2, PPND, TAU microtubule-associated protein tau C00018753
9437 NCR1, CD335, LY94, NK-p46, NKP46 natural cytotoxicity triggering receptor 1 C00018753
9436 NCR2, CD336, LY95, NK-p44, NKP44, dJ149M18.1 natural cytotoxicity triggering receptor 2 C00018753
259197 NCR3, 1C7, CD337, LY117, MALS, NKp30 natural cytotoxicity triggering receptor 3 C00018753
5578 PRKCA, AAG6, PKC-alpha, PKCA, PRKACA protein kinase C, alpha (EC:2.7.11.13) C00018753
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00018753
6194 RPS6, S6 ribosomal protein S6 C00018753
6776 STAT5A, MGF, STAT5 signal transducer and activator of transcription 5A C00018753
54600 UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) C00018753

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (72)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#103780 Alcohol dependence P08172
P14416
P31645
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
%606641 Body mass index; bmi P37231
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#218800 Crigler-najjar syndrome, type i P22309
#606785 Crigler-najjar syndrome, type ii P22309
#162800 Cyclic neutropenia P08246
#127750 Dementia, lewy body; dlb P37840
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#119900 Digital clubbing, isolated congenital P15428
#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
#143500 Gilbert syndrome P22309
#137800 Glioma susceptibility 1; glm1 P04626
P37231
#610140 Heart-hand syndrome, slovenian type P02545
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#603932 Intervertebral disc disease; idd P14780
#613837 Leber congenital amaurosis 11; lca11 P20839
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#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
#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
#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
#601665 Obesity P32245
P37231
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#607276 Resting heart rate, variation in P08588
#275210 Restrictive dermopathy, lethal P02545
#180105 Retinitis pigmentosa 10; rp10 P20839
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#190300 Tremor, hereditary essential, 1; etm1 P35462
#610379 West nile virus, susceptibility to P51681
#112100 Yt blood group antigen P22303

KEGG DISEASE (58)

KEGG name UniProt
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)
P37231 (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)
H01205 Coumarin resistance P11712 (related)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00527 Retinitis pigmentosa (RP) P20839 (related)
H00837 Leber congenital amaurosis (LCR) P20839 (related)
H00548 Brunner syndrome P21397 (related)
H00208 Hyperbilirubinemia P22309 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
Q99714 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (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

11 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000740 Anemia C00018753
D005767 Gastrointestinal Diseases C00018753
D006086 Graft vs Host Disease C00018753
D006526 Hepatitis C C00018753
D007249 Inflammation C00018753
D007968 Leukoencephalopathy, Progressive Multifocal C00018753
D007970 Leukopenia C00018753
D055953 Microscopic Polyangiitis C00018753
D009336 Necrosis C00018753
D009421 Nervous System Malformations C00018753
D014890 Wegener Granulomatosis C00018753