Species

KNApSAcK Entry

Organism name Foeniculum vulgare
Genus Foeniculum
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Foeniculum vulgare
Linked NCBI taxonomy ID 48038
Linked level species

Family

Family in NCBI taxonomy Apiaceae
ID 4037

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Natural Activity

List (54)

Species Activity
Foeniculum vulgare Mill. Abortifacient
Foeniculum vulgare Mill. Alexeteric
Foeniculum vulgare Mill. Analgesic
Foeniculum vulgare Mill. Anorectic
Foeniculum vulgare Mill. Antiandrogenic
Foeniculum vulgare Mill. Antibacterial
Foeniculum vulgare Mill. Antidopaminergic
Foeniculum vulgare Mill. Antidote
Foeniculum vulgare Mill. Antiedemic
Foeniculum vulgare Mill. Antifertility
Foeniculum vulgare Mill. Antiinflammatory
Foeniculum vulgare Mill. Antileukemic
Foeniculum vulgare Mill. Antioxidant
Foeniculum vulgare Mill. Antipyretic
Foeniculum vulgare Mill. Antiseptic
Foeniculum vulgare Mill. Antispasmodic
Foeniculum vulgare Mill. Antitussive
Foeniculum vulgare Mill. Antiviral
Foeniculum vulgare Mill. Antiwrinkle
Foeniculum vulgare Mill. Aperitif
Foeniculum vulgare Mill. Aphrodisiac
Foeniculum vulgare Mill. Bitter
Foeniculum vulgare Mill. Cardiotonic
Foeniculum vulgare Mill. Carminative
Foeniculum vulgare Mill. Choleretic
Foeniculum vulgare Mill. Cholinomimetic
Foeniculum vulgare Mill. Collyrium
Foeniculum vulgare Mill. Cytotoxic
Foeniculum vulgare Mill. Diaphoretic
Foeniculum vulgare Mill. Digestive
Foeniculum vulgare Mill. Diuretic
Foeniculum vulgare Mill. Emmenagogue
Foeniculum vulgare Mill. Estrogenic
Foeniculum vulgare Mill. Eupeptic
Foeniculum vulgare Mill. Expectorant
Foeniculum vulgare Mill. Fungicide
Foeniculum vulgare Mill. Gastrostimulant
Foeniculum vulgare Mill. Hepatoregenerative
Foeniculum vulgare Mill. Lactagogue
Foeniculum vulgare Mill. Laxative
Foeniculum vulgare Mill. Mastogenic
Foeniculum vulgare Mill. Mucogenic
Foeniculum vulgare Mill. Mutagenic
Foeniculum vulgare Mill. Mycolytic
Foeniculum vulgare Mill. Myorelaxant
Foeniculum vulgare Mill. Myostimulant
Foeniculum vulgare Mill. Narcotic
Foeniculum vulgare Mill. Pectoral
Foeniculum vulgare Mill. Secretolytic
Foeniculum vulgare Mill. Stimulant
Foeniculum vulgare Mill. Stomachic
Foeniculum vulgare Mill. Tonic
Foeniculum vulgare Mill. Vagina Protective
Foeniculum vulgare Mill. Vermifuge

Metabolite list (15)

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
C00005368 External link 512 Guaijaverin
/ Quercetin 3-O-alpha-L-arabinopyranoside
CHEMBL183031
CHEMBL185461
CHEMBL488198
CHEMBL464507
CHEMBL520637
C088178
No. 2 No. 15
C00005376 External link 512 Miquelianin
/ Quercetin 3-O-beta-D-glucuronide
CHEMBL520546
CHEMBL1506682
23 / 30 / 21 No. 2 No. 15
C00006834 External link 512 Cyanidin 3-[6-(6-sinapylglucosyl)-2-xylosylgalactoside]
No. 7 No. 15
C00006833 External link 512 Cyanidin 3-[6-(6-ferulylglucosyl)-2-xylosylgalactoside]
No. 7 No. 15
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
C00034399 External link 512 7alpha-Hydroxycampesterol
CHEMBL1784245
C079192
No. 53 No. 11
C00034466 External link 512 cis-Miyabenol C
/ (+)-cis-Miyabenol C
No. 163 No. 30
C00015825 External link 512 Miyabenol C
/ trans-Miyabenol
No. 163 No. 30
C00033008 External link 512 Glucosyringic acid
/ Syringin 4-O-beta-glucoside
C092651
No. 662
C00000010 External link 512 Syringin
CHEMBL250872
C028305
1 / 0 / 0 0 / 1 No. 678 No. 6
C00000300 External link 512 Seselin
/ Amyrolin
/ Seseline
CHEMBL71358
2 / 0 / 0 No. 750 No. 25
C00034516 External link 512 Foeniculoside X
No. 771
C00034517 External link 512 Foeniculoside XI
/ (+)-Foeniculoside XI
No. 771
C00003045 External link 512 Fenchone
/ (+)-Fenchone
C027327
No. 1921 No. 35
C00002713 External link 512 Anethole
CHEMBL452630
CHEMBL1468832
C006578
6 / 21 / 49 16 / 13 No. 2748 No. 6

Human Protein / Gene in interactions

54 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P06746 DNA polymerase beta Enzyme C00005376 C00019064 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002713 C00005376 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00005376 C00019064 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00005376 C00019064 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00005376 C00019064 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002713 C00005376 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000010 C00019064 0 / 0
P02545 Prelamin-A/C Unclassified protein C00002713 C00005376 11 / 10
P09923 Intestinal-type alkaline phosphatase Enzyme C00005376 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00005376 0 / 0
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
Q06124 Tyrosine-protein phosphatase non-receptor type 11 Tyr C00019064 4 / 2
P16473 Thyrotropin receptor Glycohormone receptor C00002713 3 / 2
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00019064 0 / 0
P10586 Receptor-type tyrosine-protein phosphatase F Receptor tyrosine-protein phosphatase C00019064 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00005376 1 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00005376 1 / 1
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00019064 0 / 0
P39748 Flap endonuclease 1 Enzyme C00005376 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00019064 0 / 0
O75496 Geminin Unclassified protein C00019064 0 / 0
P15121 Aldose reductase Enzyme C00019064 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00019064 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00005376 7 / 3
Q9Y253 DNA polymerase eta Enzyme C00005376 1 / 1
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00000300 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00005376 3 / 1
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00019064 0 / 3
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00019064 2 / 2
Q96RI1 Bile acid receptor NR1H4 C00019064 0 / 0
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
P10696 Alkaline phosphatase, placental-like Enzyme C00005376 0 / 1
P56817 Beta-secretase 1 A1A C00000300 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00019064 0 / 0
P35228 Nitric oxide synthase, inducible Enzyme C00019064 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002713 0 / 1
O60218 Aldo-keto reductase family 1 member B10 Enzyme C00019064 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00005376 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00005376 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00005376 4 / 3
P17706 Tyrosine-protein phosphatase non-receptor type 2 Tyr C00019064 0 / 1
P29350 Tyrosine-protein phosphatase non-receptor type 6 Tyr C00019064 0 / 0
P04054 Phospholipase A2 Enzyme C00019064 0 / 0
P23469 Receptor-type tyrosine-protein phosphatase epsilon Receptor tyrosine-protein phosphatase C00019064 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00005376 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00002713 7 / 37
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00005376 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00019064 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00019064 1 / 4
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00005376 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00005376 2 / 1

34 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00002713 C00019064
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00002713 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) C00002713 C00019064
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00019064
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00002713
3551 IKBKB, IKK-beta, IKK2, IKKB, NFKBIKB inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta (EC:2.7.11.10) C00002713
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00002713
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) C00002713
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00002713
4790 NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 C00002713
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002713
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00002713
5328 PLAU, ATF, BDPLT5, QPD, UPA, URK, u-PA plasminogen activator, urokinase (EC:3.4.21.73) C00002713
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002713
7076 TIMP1, CLGI, EPA, EPO, HCI, TIMP TIMP metallopeptidase inhibitor 1 C00002713
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00002713
177 AGER, RAGE advanced glycosylation end product-specific receptor C00019064
5604 MAP2K1, CFC3, MAPKK1, MEK1, MKK1, PRKMK1 mitogen-activated protein kinase kinase 1 (EC:2.7.12.2) C00002713
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
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
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 (48)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc Q14191
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#607785 Juvenile myelomonocytic leukemia; jmml Q06124
#151100 Leopard syndrome 1 Q06124
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#211980 Lung cancer P04637
#611162 Malaria, susceptibility to P35228
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#156250 Metachondromatosis; metcds Q06124
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#163950 Noonan syndrome 1; ns1 Q06124
#166350 Osseous heteroplasia, progressive; poh P63092
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#275210 Restrictive dermopathy, lethal P02545
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (68)

KEGG name UniProt
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)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (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)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
P35228 (related)
P35354 (related)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
P35354 (related)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast 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)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
P35354 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00213 Hypophosphatasia P05186 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00023 Testicular cancer P10696 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00408 Type I diabetes mellitus P17706 (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) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00523 Noonan syndrome and related disorders Q06124 (related)
H01018 Metachondromatosis Q06124 (related)
H00296 Defects in RecQ helicases Q14191 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

26 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D056486 Drug-Induced Liver Injury C00002713
C00019064
D008107 Liver Diseases C00002713
C00019064
D007249 Inflammation C00002713
C00019064
D001862 Bone Resorption C00000010
D005767 Gastrointestinal Diseases C00002713
D007022 Hypotension C00002713
D003877 Dermatitis, Contact C00002713
D002286 Carcinoma, Ehrlich Tumor C00002713
D008113 Liver Neoplasms C00002713
D009362 Neoplasm Metastasis C00002713
D010243 Paralysis C00002713
D013276 Stomach Ulcer C00002713
D013927 Thrombosis C00002713
D001919 Bradycardia C00002713
D002252 Carbon Tetrachloride Poisoning C00019064
D050171 Dyslipidemias C00019064
D018149 Glucose Intolerance C00019064
D006949 Hyperlipidemias C00019064
D007674 Kidney Diseases C00019064
D008103 Liver Cirrhosis C00019064
D008106 Liver Cirrhosis, Experimental C00019064
D017202 Myocardial Ischemia C00019064
D009369 Neoplasms C00019064
D009765 Obesity C00019064
D011041 Poisoning C00019064
D011230 Precancerous Conditions C00019064