Streptomyces violaceus P950-4 (ATCC 53807)
Species
KNApSAcK Entry
| Organism name | Streptomyces violaceus P950-4 (ATCC 53807) |
|---|---|
| Genus | Streptomyces |
| Family | Streptomycetaceae |
| Kingdom | Bacteria |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Streptomyces |
|---|---|
| Linked NCBI taxonomy ID | 1883 |
| Linked level | genus |
Family
| Family in NCBI taxonomy | Streptomycetaceae |
|---|---|
| ID | 2062 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Bacteria |
|---|---|
| ID | 2 |
Plant class
| Plant class | |
|---|---|
| ID |
Metabolite list (1)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00017127
|
Unidox
/ GS 3065 / Doxycen / Monodox / Ronaxan / Doxinyl / Liviatin / Pulmodox / Tolexine / Doxivetin / Dentistar / Hydramycin / Vibramycin / Medeomycin / Vibravenos / Vibramycine / Doxycycline / Deoxymykoin / Vibranos SF / Vibraveineuse / Doxytetracycline / alpha-Doxycycline / 6-Deoxyoxytetracycline / alpha-6-Deoxyoxytetracycline |
CHEMBL1433
CHEMBL1372176 CHEMBL1616405 CHEMBL1624566 |
D004318
|
114 / 51 / 40 | 14 / 102 | No. 5500 |
|
Human Protein / Gene in interactions
114 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00017127 | 1 / 0 |
| P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00017127 | 2 / 0 |
| P21728 | D(1A) dopamine receptor | Dopamine receptor | C00017127 | 0 / 0 |
| P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00017127 | 0 / 3 |
| Q12809 | Potassium voltage-gated channel subfamily H member 2 | KCNH, Kv10-12.x (Ether-a-go-go) | C00017127 | 2 / 2 |
| P08246 | Neutrophil elastase | S1A | C00017127 | 2 / 1 |
| P33765 | Adenosine receptor A3 | Adenosine receptor | C00017127 | 0 / 0 |
| Q16539 | Mitogen-activated protein kinase 14 | p38 | C00017127 | 0 / 0 |
| P49146 | Neuropeptide Y receptor type 2 | Neuropeptide Y receptor | C00017127 | 0 / 0 |
| P22894 | Neutrophil collagenase | M10A | C00017127 | 0 / 0 |
| P29466 | Caspase-1 | C14 | C00017127 | 0 / 0 |
| P17252 | Protein kinase C alpha type | Alpha | C00017127 | 0 / 0 |
| P27361 | Mitogen-activated protein kinase 3 | Erk | C00017127 | 0 / 0 |
| P14780 | Matrix metalloproteinase-9 | M10A | C00017127 | 2 / 2 |
| O15245 | Solute carrier family 22 member 1 | Drug uniporter | C00017127 | 0 / 0 |
| O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00017127 | 0 / 0 |
| P16473 | Thyrotropin receptor | Glycohormone receptor | C00017127 | 3 / 2 |
| P00918 | Carbonic anhydrase 2 | Lyase | C00017127 | 1 / 2 |
| P07550 | Beta-2 adrenergic receptor | Adrenergic receptor | C00017127 | 0 / 1 |
| P21397 | Amine oxidase [flavin-containing] A | Oxidoreductase | C00017127 | 1 / 1 |
| P25021 | Histamine H2 receptor | Histamine receptor | C00017127 | 0 / 0 |
| P35367 | Histamine H1 receptor | Histamine receptor | C00017127 | 0 / 0 |
| Q01959 | Sodium-dependent dopamine transporter | Dopamine | C00017127 | 1 / 0 |
| P08912 | Muscarinic acetylcholine receptor M5 | Acetylcholine receptor | C00017127 | 0 / 0 |
| P18825 | Alpha-2C adrenergic receptor | Adrenergic receptor | C00017127 | 0 / 0 |
| P13945 | Beta-3 adrenergic receptor | Adrenergic receptor | C00017127 | 0 / 0 |
| P02768 | Serum albumin | Secreted protein | C00017127 | 0 / 0 |
| P25024 | C-X-C chemokine receptor type 1 | CXC chemokine receptor | C00017127 | 0 / 0 |
| P06241 | Tyrosine-protein kinase Fyn | Src | C00017127 | 0 / 0 |
| Q08209 | Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform | Ser_Thr | C00017127 | 0 / 0 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00017127 | 0 / 1 |
| P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00017127 | 1 / 8 |
| P11473 | Vitamin D3 receptor | NR1I1 | C00017127 | 2 / 3 |
| P14416 | D(2) dopamine receptor | Dopamine receptor | C00017127 | 2 / 0 |
| P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00017127 | 0 / 0 |
| P37288 | Vasopressin V1a receptor | Vasopressin and oxytocin receptor | C00017127 | 0 / 0 |
| P41145 | Kappa-type opioid receptor | Opioid receptor | C00017127 | 0 / 0 |
| Q9Y271 | Cysteinyl leukotriene receptor 1 | Leukotriene receptor | C00017127 | 0 / 0 |
| P29274 | Adenosine receptor A2a | Adenosine receptor | C00017127 | 0 / 0 |
| P25929 | Neuropeptide Y receptor type 1 | Neuropeptide Y receptor | C00017127 | 0 / 0 |
| P50052 | Type-2 angiotensin II receptor | Angiotensin receptor | C00017127 | 1 / 1 |
| P17948 | Vascular endothelial growth factor receptor 1 | Vegfr | C00017127 | 0 / 0 |
| P41968 | Melanocortin receptor 3 | Melanocortin receptor | C00017127 | 1 / 0 |
| P11509 | Cytochrome P450 2A6 | Cytochrome P450 2A6 | C00017127 | 0 / 0 |
| Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00017127 | 0 / 0 |
| P39748 | Flap endonuclease 1 | Enzyme | C00017127 | 0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00017127 | 0 / 0 |
| Q8TCC7 | Solute carrier family 22 member 8 | Antiporter | C00017127 | 0 / 0 |
| P04035 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase | Oxidoreductase | C00017127 | 0 / 0 |
| P08913 | Alpha-2A adrenergic receptor | Adrenergic receptor | C00017127 | 0 / 0 |
| P21917 | D(4) dopamine receptor | Dopamine receptor | C00017127 | 0 / 0 |
| P30988 | Calcitonin receptor | Calcitonin receptor | C00017127 | 0 / 0 |
| P35462 | D(3) dopamine receptor | Dopamine receptor | C00017127 | 1 / 0 |
| P41143 | Delta-type opioid receptor | Opioid receptor | C00017127 | 0 / 0 |
| Q92731 | Estrogen receptor beta | NR3A2 | C00017127 | 0 / 1 |
| P41595 | 5-hydroxytryptamine receptor 2B | Serotonin receptor | C00017127 | 0 / 0 |
| P25101 | Endothelin-1 receptor | Endothelin receptor | C00017127 | 0 / 0 |
| P30411 | B2 bradykinin receptor | Bradykinin receptor | C00017127 | 0 / 0 |
| P32245 | Melanocortin receptor 4 | Melanocortin receptor | C00017127 | 1 / 0 |
| P32238 | Cholecystokinin receptor type A | Cholecystokinin receptor | C00017127 | 0 / 0 |
| P08311 | Cathepsin G | S1A | C00017127 | 0 / 0 |
| Q99720 | Sigma non-opioid intracellular receptor 1 | Membrane receptor | C00017127 | 1 / 0 |
| P03956 | Interstitial collagenase | M10A | C00017127 | 0 / 1 |
| P32241 | Vasoactive intestinal polypeptide receptor 1 | Vasoactive intestinal peptide receptor | C00017127 | 0 / 0 |
| P55085 | Proteinase-activated receptor 2 | Protease-activated receptor | C00017127 | 0 / 0 |
| Q4U2R8 | Solute carrier family 22 member 6 | Antiporter | C00017127 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00017127 | 0 / 0 |
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00017127 | 0 / 0 |
| P04150 | Glucocorticoid receptor | NR3C1 | C00017127 | 0 / 1 |
| P08172 | Muscarinic acetylcholine receptor M2 | Acetylcholine receptor | C00017127 | 2 / 0 |
| P11229 | Muscarinic acetylcholine receptor M1 | Acetylcholine receptor | C00017127 | 0 / 0 |
| P21554 | Cannabinoid receptor 1 | Cannabinoid receptor | C00017127 | 0 / 0 |
| P31645 | Sodium-dependent serotonin transporter | Serotonin | C00017127 | 2 / 0 |
| P04626 | Receptor tyrosine-protein kinase erbB-2 | TK tyrosine-protein kinase EGFR subfamily | C00017127 | 5 / 9 |
| P20309 | Muscarinic acetylcholine receptor M3 | Acetylcholine receptor | C00017127 | 1 / 0 |
| P21452 | Substance-K receptor | Neurokinin receptor | C00017127 | 0 / 0 |
| P51679 | C-C chemokine receptor type 4 | CC chemokine receptor | C00017127 | 0 / 0 |
| P51681 | C-C chemokine receptor type 5 | CC chemokine receptor | C00017127 | 3 / 0 |
| P50406 | 5-hydroxytryptamine receptor 6 | Serotonin receptor | C00017127 | 0 / 0 |
| P45452 | Collagenase 3 | M10A | C00017127 | 1 / 1 |
| P41597 | C-C chemokine receptor type 2 | CC chemokine receptor | C00017127 | 1 / 0 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00017127 | 0 / 0 |
| P08575 | Receptor-type tyrosine-protein phosphatase C | Enzyme | C00017127 | 2 / 1 |
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00017127 | 0 / 0 |
| P08253 | 72 kDa type IV collagenase | M10A | C00017127 | 1 / 3 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00017127 | 3 / 3 |
| O76074 | cGMP-specific 3',5'-cyclic phosphodiesterase | PDE_5A | C00017127 | 0 / 0 |
| P03372 | Estrogen receptor | NR3A1 | C00017127 | 1 / 1 |
| P08588 | Beta-1 adrenergic receptor | Adrenergic receptor | C00017127 | 1 / 0 |
| P22303 | Acetylcholinesterase | Hydrolase | C00017127 | 1 / 0 |
| P28223 | 5-hydroxytryptamine receptor 2A | Serotonin receptor | C00017127 | 0 / 0 |
| P28335 | 5-hydroxytryptamine receptor 2C | Serotonin receptor | C00017127 | 0 / 0 |
| P35372 | Mu-type opioid receptor | Opioid receptor | C00017127 | 0 / 0 |
| P08173 | Muscarinic acetylcholine receptor M4 | Acetylcholine receptor | C00017127 | 0 / 0 |
| P25103 | Substance-P receptor | Neurokinin receptor | C00017127 | 0 / 0 |
| P25105 | Platelet-activating factor receptor | PAF receptor | C00017127 | 0 / 0 |
| P33032 | Melanocortin receptor 5 | Melanocortin receptor | C00017127 | 0 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00017127 | 1 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00017127 | 0 / 1 |
| P05181 | Cytochrome P450 2E1 | Cytochrome P450 2E1 | C00017127 | 0 / 0 |
| Q9UM07 | Protein-arginine deiminase type-4 | Enzyme | C00017127 | 1 / 0 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00017127 | 0 / 0 |
| P23975 | Sodium-dependent noradrenaline transporter | Norepinephrine | C00017127 | 1 / 1 |
| P25100 | Alpha-1D adrenergic receptor | Adrenergic receptor | C00017127 | 0 / 0 |
| P30542 | Adenosine receptor A1 | Adenosine receptor | C00017127 | 0 / 0 |
| P18089 | Alpha-2B adrenergic receptor | Adrenergic receptor | C00017127 | 0 / 0 |
| P24557 | Thromboxane-A synthase | Cytochrome P450 5A1 | C00017127 | 1 / 1 |
| P06239 | Tyrosine-protein kinase Lck | Src | C00017127 | 0 / 1 |
| P25025 | C-X-C chemokine receptor type 2 | CXC chemokine receptor | C00017127 | 0 / 0 |
| P08254 | Stromelysin-1 | M10A | C00017127 | 1 / 0 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00017127 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00017127 | 0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00017127 | 1 / 1 |
| Q9NSA0 | Solute carrier family 22 member 11 | Transporter | C00017127 | 0 / 0 |
14 Gene in CTD interactions
| gene | gene name | gene description | KNApSAcK metabolite in interactions |
|---|---|---|---|
| 5243 | ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 | ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) |
C00017127
|
| 196 | AHR, bHLHe76 | aryl hydrocarbon receptor |
C00017127
|
| 1545 | CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 | cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) |
C00017127
|
| 3553 | IL1B, IL-1, IL1-BETA, IL1F2 | interleukin 1, beta |
C00017127
|
| 3576 | IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 | interleukin 8 |
C00017127
|
| 4322 | MMP13, CLG3, MANDP1 | matrix metallopeptidase 13 (collagenase 3) (EC:3.4.24.-) |
C00017127
|
| 4313 | MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1 | matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (EC:3.4.24.24) |
C00017127
|
| 4314 | MMP3, CHDS6, MMP-3, SL-1, STMY, STMY1, STR1 | matrix metallopeptidase 3 (stromelysin 1, progelatinase) (EC:3.4.24.17) |
C00017127
|
| 4317 | MMP8, CLG1, HNC, MMP-8, PMNL-CL | matrix metallopeptidase 8 (neutrophil collagenase) (EC:3.4.24.34) |
C00017127
|
| 4318 | MMP9, CLG4B, GELB, MANDP2, MMP-9 | matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) |
C00017127
|
| 9356 | SLC22A6, HOAT1, OAT1, PAHT, ROAT1 | solute carrier family 22 (organic anion transporter), member 6 |
C00017127
|
| 7124 | TNF, DIF, TNF-alpha, TNFA, TNFSF2 | tumor necrosis factor |
C00017127
|
| 54575 | UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J | UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) |
C00017127
|
| 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) |
C00017127
|
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (51)
| 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 |
| #614373 | Amyotrophic lateral sclerosis 16, juvenile; als16 |
Q99720
|
| #602025 | Body mass index quantitative trait locus 9; bmiq9 |
P41968
|
| #300615 | Brunner syndrome |
P21397
|
| #614466 | Coronary heart disease, susceptibility to, 6; chds6 |
P08254
|
| #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
|
| #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
|
| #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
|
| #613688 | Long qt syndrome 2; lqt2 |
Q12809
|
| #211980 | Lung cancer |
P00533
P04626 |
| #608516 | Major depressive disorder; mdd |
P08172
|
| #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
|
| #259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona |
P08253
|
| #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
|
| #259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
| #167000 | Ovarian cancer |
P04626
|
| #613135 | Parkinsonism-dystonia, infantile; pkdys |
Q01959
|
| #607276 | Resting heart rate, variation in |
P08588
|
| #180300 | Rheumatoid arthritis; ra |
Q9UM07
|
| #604906 | Schizophrenia 9; sczd9 |
P49798
|
| #181500 | Schizophrenia; sczd |
P49798
|
| #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
|
| #602111 | Spondyloepimetaphyseal dysplasia, missouri type |
P45452
|
| #190300 | Tremor, hereditary essential, 1; etm1 |
P35462
|
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
| #610379 | West nile virus, susceptibility to |
P51681
|
| #112100 | Yt blood group antigen |
P22303
|
KEGG DISEASE (40)
| 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) P08253 (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)
|
| 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)
|
| H00025 | Penile cancer |
P08253
(related)
P14780 (related) P35354 (related) |
| H00472 | Torg-Winchester syndrome |
P08253
(related)
|
| H00091 | T-B+Severe combined immunodeficiencies (SCIDs) |
P08575
(related)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| 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)
P45452 (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)
|
| H00480 | Non-syndromic X-linked mental retardation |
P50052
(related)
Q99714 (related) |
| H00720 | Long QT syndrome |
Q12809
(related)
|
| H00725 | Short QT syndrome |
Q12809
(related)
|
| H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|
Diseases related to CTD interactions
102 disease in interactions with metabolites
| MESH or OMIM | name |
KNApSAcK
metabolite |
|---|---|---|
| D015746 | Abdominal Pain |
C00017127
|
| D017486 | Acneiform Eruptions |
C00017127
|
| D000152 | Acne Vulgaris |
C00017127
|
| D000647 | Amnesia |
C00017127
|
| D000783 | Aneurysm |
C00017127
|
| D001008 | Anxiety Disorders |
C00017127
|
| D001019 | Aortic Rupture |
C00017127
|
| D001072 | Apraxias |
C00017127
|
| D001416 | Back Pain |
C00017127
|
| D001660 | Biliary Tract Diseases |
C00017127
|
| D001943 | Breast Neoplasms |
C00017127
|
| D001991 | Bronchitis |
C00017127
|
| D029481 | Bronchitis, Chronic |
C00017127
|
| D002177 | Candidiasis |
C00017127
|
| D006332 | Cardiomegaly |
C00017127
|
| D002637 | Chest Pain |
C00017127
|
| D002690 | Chlamydia Infections |
C00017127
|
| D016770 | Ciliophora Infections |
C00017127
|
| D019970 | Cocaine-Related Disorders |
C00017127
|
| D017714 | Community-Acquired Infections |
C00017127
|
| D003711 | Demyelinating Diseases |
C00017127
|
| D003715 | Dengue |
C00017127
|
| D003866 | Depressive Disorder |
C00017127
|
| D003967 | Diarrhea |
C00017127
|
| D004184 | Dirofilariasis |
C00017127
|
| D006970 | Disorders of Excessive Somnolence |
C00017127
|
| D004244 | Dizziness |
C00017127
|
| D003875 | Drug Eruptions |
C00017127
|
| D004342 | Drug Hypersensitivity |
C00017127
|
| D056486 | Drug-Induced Liver Injury |
C00017127
|
| D064420 | Drug-Related Side Effects and Adverse Reactions |
C00017127
|
| D004401 | Dysarthria |
C00017127
|
| D004697 | Endocarditis, Bacterial |
C00017127
|
| D004802 | Eosinophilia |
C00017127
|
| C538499 | Erythema migrans |
C00017127
|
| D005076 | Exanthema |
C00017127
|
| D005128 | Eye Diseases |
C00017127
|
| D005221 | Fatigue |
C00017127
|
| D005393 | Fish Diseases |
C00017127
|
| D005402 | Fistula |
C00017127
|
| D020234 | Gait Ataxia |
C00017127
|
| D005767 | Gastrointestinal Diseases |
C00017127
|
| D006192 | Haemophilus Infections |
C00017127
|
| D006261 | Headache |
C00017127
|
| D034381 | Hearing Loss |
C00017127
|
| D006606 | Hiccup |
C00017127
|
| D006943 | Hyperglycemia |
C00017127
|
| D006973 | Hypertension |
C00017127
|
| D006987 | Hypesthesia |
C00017127
|
| D007010 | Hyponatremia |
C00017127
|
| D017674 | Hypophosphatemia |
C00017127
|
| D019586 | Intracranial Hypertension |
C00017127
|
| D007970 | Leukopenia |
C00017127
|
| D008107 | Liver Diseases |
C00017127
|
| D017114 | Liver Failure, Acute |
C00017127
|
| D008193 | Lyme Disease |
C00017127
|
| D008223 | Lymphoma |
C00017127
|
| D008231 | Lymphopenia |
C00017127
|
| D008288 | Malaria |
C00017127
|
| D008382 | Marfan Syndrome |
C00017127
|
| D008569 | Memory Disorders |
C00017127
|
| D009120 | Muscle Cramp |
C00017127
|
| D009325 | Nausea |
C00017127
|
| D009422 | Nervous System Diseases |
C00017127
|
| D009503 | Neutropenia |
C00017127
|
| D000857 | Olfaction Disorders |
C00017127
|
| D009896 | Optic Atrophy |
C00017127
|
| D010003 | Osteoarthritis |
C00017127
|
| D010211 | Papilledema |
C00017127
|
| D010243 | Paralysis |
C00017127
|
| D010292 | Paresthesia |
C00017127
|
| D034161 | Pelvic Infection |
C00017127
|
| D010391 | Pemphigoid, Bullous |
C00017127
|
| D010518 | Periodontitis |
C00017127
|
| D010689 | Phlebitis |
C00017127
|
| D010787 | Photosensitivity Disorders |
C00017127
|
| D010859 | Pigmentation Disorders |
C00017127
|
| D011008 | Pneumococcal Infections |
C00017127
|
| D011014 | Pneumonia |
C00017127
|
| D011115 | Polyneuropathies |
C00017127
|
| D011475 | Prosthesis Failure |
C00017127
|
| D011507 | Proteinuria |
C00017127
|
| D011537 | Pruritus |
C00017127
|
| D011559 | Pseudotumor Cerebri |
C00017127
|
| D011625 | Pterygium |
C00017127
|
| D012141 | Respiratory Tract Infections |
C00017127
|
| D012393 | Rosacea |
C00017127
|
| D012640 | Seizures |
C00017127
|
| D012871 | Skin Diseases |
C00017127
|
| D012874 | Skin Diseases, Infectious |
C00017127
|
| D013492 | Suppuration |
C00017127
|
| D013575 | Syncope |
C00017127
|
| D013587 | Syphilis |
C00017127
|
| D014075 | Tooth Discoloration |
C00017127
|
| D014202 | Tremor |
C00017127
|
| D014526 | Urethritis |
C00017127
|
| D014552 | Urinary Tract Infections |
C00017127
|
| D002575 | Uterine Cervicitis |
C00017127
|
| D014623 | Vaginal Diseases |
C00017127
|
| D018366 | Vasculitis, Leukocytoclastic, Cutaneous |
C00017127
|
| D015354 | Vision, Low |
C00017127
|
| D014839 | Vomiting |
C00017127
|