| class name | count |
|---|---|
| Magnoliophyta | 28 |
| asterids | 24 |
| rosids | 20 |
| Liliopsida | 11 |
| Euphyllophyta | 9 |
| eudicotyledons | 5 |
| Spermatophyta | 2 |
| class name | count |
|---|---|
|
Annonaceae
|
17 |
|
Asteraceae
|
11 |
|
Pteridaceae
|
9 |
|
Gesneriaceae
|
8 |
|
Fabaceae
|
7 |
|
Zingiberaceae
|
7 |
|
Rutaceae
|
5 |
|
Lauraceae
|
5 |
|
Piperaceae
|
5 |
|
Polygonaceae
|
5 |
|
Lamiaceae
|
3 |
|
Orchidaceae
|
2 |
|
Acanthaceae
|
2 |
|
Pinaceae
|
2 |
|
Combretaceae
|
2 |
|
Rosaceae
|
2 |
|
Salicaceae
|
1 |
|
Cannabaceae
|
1 |
|
Xanthorrhoeaceae
|
1 |
|
Myristicaceae
|
1 |
| br08003 Category | # of metabolite |
|---|
| br08003 Category | KEGG ID | KNApSAcK ID |
|---|
| KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
|---|---|---|---|---|---|---|
|
C00006923
|
Glypallichalcone
/ 4-Hydroxy-2,4'-dimethoxychalcone |
C079973
|
|
|||
|
C00006929
|
Isoliquiritigenin 4,4'-dimethyl ether
|
CHEMBL229907
|
18 / 36 / 28 |
|
||
|
C00006936
|
Flavokawin B
|
CHEMBL104255
|
19 / 31 / 55 |
|
||
|
C00006937
|
Tepanone
|
|
||||
|
C00006939
|
2,4-Dihydroxy-6,4'-dimethoxychalcone
|
|
||||
|
C00006946
|
2',4'-Dihydroxy-3,4-dimethoxychalcone
|
CHEMBL573524
|
19 / 38 / 59 |
|
||
|
C00006950
|
Kukulkanin A
|
C061638
|
|
|||
|
C00006955
|
Gymnogrammene
|
|
||||
|
C00006956
|
4,4'-Dihydroxy-2',6'-dimethoxychalcone
|
CHEMBL449907
|
|
|||
|
C00006957
|
Flavokawain C
|
CHEMBL251958
|
|
|||
|
C00006958
|
Flavokawin A
/ 2'-Hydroxy-4,4',6'-trimethoxychalcone |
CHEMBL243829
|
3 / 3 / 0 |
|
||
|
C00006959
|
Pashanone
|
|
||||
|
C00006960
|
2',4'-Dihydroxy-3',6'-dimethoxychalcone
|
|
||||
|
C00006961
|
2',3'-Dihydroxy-4',6'-dimethoxychalcone
|
CHEMBL1446527
|
13 / 17 / 11 |
|
||
|
C00006962
|
Helilandin B
|
|
||||
|
C00006963
|
2'-Hydroxy-3',4',6'-trimethoxychalcone
|
|
||||
|
C00006964
|
2',3',4',6'-Tetramethoxychalcone
|
|
||||
|
C00006965
|
Cerasin
|
CHEMBL601679
|
|
|||
|
C00006966
|
Cerasidin
|
|
||||
|
C00006967
|
2',4'-Dihydroxy-2,3',6'-trimethoxychalcone
|
|
||||
|
C00006971
|
Okanin 3,4,3',4'-tetramethyl ether
|
CHEMBL316850
CHEMBL1702432 |
11 / 8 / 9 |
|
||
|
C00006976
|
3,2'-Dihydroxy-4,4',6'-trimethoxychalcone
|
CHEMBL571087
|
15 / 19 / 52 |
|
||
|
C00006977
|
2'-Hydroxy-3,4,4',6'-tetramethoxychalcone
|
CHEMBL243830
|
3 / 3 / 0 |
|
||
|
C00006979
|
4,6'-Dihydroxy-2',3',4'-trimethoxychalcone
|
CHEMBL2208192
|
|
|||
|
C00006980
|
4,2'-Dihydroxy-3',4',6'-trimethoxychalcone
|
|
||||
|
C00006981
|
6'-Hydroxy-4,2',3',4'-tetramethoxychalcone
|
CHEMBL2208193
|
1 / 5 / 3 |
|
||
|
C00006982
|
Pedicin
/ 2',5'-Dihydroxy-3',4',6'-trimethoxychalcone |
CHEMBL481972
|
|
|||
|
C00006983
|
Isodidymocarpin
|
CHEMBL505666
|
|
|||
|
C00006984
|
3'-Hydroxy-2',4',5',6'-tetramethoxychalcone
|
|
||||
|
C00006985
|
Kanakugiol
|
|
||||
|
C00006986
|
Pedicellin
|
CHEMBL1998453
|
|
|||
|
C00006987
|
Rubone
|
|
||||
|
C00006988
|
2'-Hydroxy-3,4,5,4',6'-pentamethoxychalcone
|
CHEMBL571877
|
1 / 2 / 0 |
|
||
|
C00006989
|
6'-Hydroxy-3,4,2',3',4'-pentamethoxychalcone
|
CHEMBL458376
|
|
|||
|
C00006990
|
2',5'-Dihydroxy-4,3',4',6'-tetramethoxychalcone
|
|
||||
|
C00014421
|
Heliannone A
/ 2',4-Dihydroxy-3',4'-dimethoxychalcone |
|
||||
|
C00014423
|
2'-Hydroxy-2,4',6'-trimethoxychalcone
|
CHEMBL258497
|
1 / 2 / 0 |
|
||
|
C00014424
|
2',4'-Dihydroxy-4,6'-dimethoxychalcone
|
CHEMBL494264
|
|
|||
|
C00014425
|
3'-Bromo-6'-hydroxy-2',4,4'-trimethoxychalcone
|
|
||||
|
C00014426
|
4'-Hydroxy-2',4,6'-trimethoxychalcone
|
CHEMBL1514861
|
2 / 3 / 4 |
|
||
|
C00014428
|
Crotaoprostrin
/ 2'-Hydroxy-3,4,5-methoxychalcone |
CHEMBL521653
|
16 / 23 / 18 |
|
||
|
C00014430
|
2'-Hydroxy-2,3,4',6'-tetramethoxychalcone
|
CHEMBL1254091
|
1 / 5 / 5 |
|
||
|
C00014433
|
4,3'-Hydroxy-2',4',5',6'-methoxychalcone
|
|
||||
|
C00014434
|
Hamilcone
/ 3,4,6'-Trihydroxy-2',3',4'-trimethoxychalcone |
CHEMBL465364
|
|
|||
|
C00014435
|
2'-Hydroxy-3',4',6',3,4-pentamethoxychalcone
|
|
||||
|
C00014436
|
2,3,4,2',4',6'-Hexamethoxychalcone
|
CHEMBL595815
|
|
|||
|
C00032628
|
2'-Hydroxy-3,4,3',4',6'-pentamethoxychalcone
|
|
||||
|
C00036451
|
2',3'-Dihydroxy-4',6'-dimethoxychalcone
|
CHEMBL1446527
|
13 / 17 / 11 |
|
||
|
C00036493
|
2'-Hydroxy-4,4',6'-trimethoxychalcone
|
CHEMBL243829
|
3 / 3 / 0 |
|
||
|
C00037157
|
Flavokavin A
/ Flavokawain A |
CHEMBL243829
|
3 / 3 / 0 |
|
||
|
C00044793
|
Guieranone A
|
CHEMBL477526
|
|
|||
|
C00045544
|
2'-Hydroxy-4',6'-dimethoxychalcone
|
CHEMBL104255
|
19 / 31 / 55 |
|
||
|
C00048940
|
2'-Hydroxy-4',5',6'-trimethoxychalcone
|
|
||||
|
C00048941
|
2'-Hydroxy-4',6'-dimethoxychalcone
|
CHEMBL104255
|
19 / 31 / 55 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00006929 C00006936 C00006946 C00006958 C00006977 C00006988 C00014423 C00036493 C00037157 C00045544 C00048941 | 2 / 0 |
| P11473 | Vitamin D3 receptor | NR1I1 | C00006936 C00006946 C00006961 C00006971 C00006976 C00014426 C00014428 C00036451 C00045544 C00048941 | 2 / 3 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00006929 C00006936 C00006946 C00006961 C00006976 C00014428 C00036451 C00045544 C00048941 | 4 / 3 |
| O75496 | Geminin | Unclassified protein | C00006929 C00006936 C00006961 C00006971 C00014428 C00036451 C00045544 C00048941 | 0 / 0 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00006936 C00006961 C00006971 C00014428 C00036451 C00045544 C00048941 | 0 / 0 |
| P33527 | Multidrug resistance-associated protein 1 | drugs | C00006929 C00006946 C00006958 C00006977 C00036493 C00037157 | 0 / 0 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00006929 C00006936 C00006946 C00006976 C00045544 C00048941 | 1 / 2 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00006929 C00006936 C00006961 C00036451 C00045544 C00048941 | 7 / 3 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00006929 C00006936 C00006946 C00006976 C00045544 C00048941 | 0 / 1 |
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00006936 C00006961 C00014428 C00036451 C00045544 C00048941 | 0 / 0 |
| P08183 | Multidrug resistance protein 1 | drug | C00006929 C00006946 C00006958 C00006977 C00036493 C00037157 | 1 / 0 |
| P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00006936 C00006946 C00014428 C00045544 C00048941 | 0 / 0 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00006929 C00006961 C00006971 C00014428 C00036451 | 1 / 1 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00006929 C00006936 C00014428 C00045544 C00048941 | 0 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00006936 C00006961 C00036451 C00045544 C00048941 | 1 / 1 |
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00006936 C00006971 C00014428 C00045544 C00048941 | 1 / 0 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00006929 C00006961 C00006971 C00014428 C00036451 | 0 / 0 |
| P04637 | Cellular tumor antigen p53 | Transcription Factor | C00006936 C00006946 C00006976 C00045544 C00048941 | 7 / 37 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00006936 C00014428 C00045544 C00048941 | 2 / 0 |
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00006936 C00006976 C00045544 C00048941 | 0 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00006946 C00006976 C00014428 | 0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00006946 C00006976 C00014426 | 1 / 1 |
| Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00006936 C00045544 C00048941 | 1 / 4 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00006929 C00006961 C00036451 | 0 / 0 |
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00006961 C00014428 C00036451 | 0 / 0 |
| O00255 | Menin | Unclassified protein | C00006929 C00006946 C00006976 | 2 / 5 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00006936 C00045544 C00048941 | 0 / 0 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00006929 C00006946 C00006976 | 0 / 0 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00006936 C00045544 C00048941 | 3 / 3 |
| Q16637 | Survival motor neuron protein | Unclassified protein | C00006929 C00006946 | 4 / 1 |
| P37231 | Peroxisome proliferator-activated receptor gamma | NR1C3 | C00006946 C00006981 | 5 / 3 |
| P02545 | Prelamin-A/C | Unclassified protein | C00006929 C00014428 | 11 / 10 |
| Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00006961 C00036451 | 1 / 0 |
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00006946 C00006976 | 2 / 2 |
| Q9Y253 | DNA polymerase eta | Enzyme | C00006961 C00036451 | 1 / 1 |
| P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00006946 C00006976 | 0 / 0 |
| P18054 | Arachidonate 12-lipoxygenase, 12S-type | Enzyme | C00006946 | 2 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00006971 | 0 / 0 |
| P37840 | Alpha-synuclein | Unclassified protein | C00006971 | 4 / 2 |
| P04062 | Glucosylceramidase | Enzyme | C00006946 | 6 / 4 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00006929 | 1 / 1 |
| O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00006976 | 0 / 0 |
| P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | C00006929 | 2 / 2 |
| O14746 | Telomerase reverse transcriptase | Enzyme | C00014430 | 5 / 5 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00006976 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00014428 | 0 / 0 |
| P39748 | Flap endonuclease 1 | Enzyme | C00006971 | 0 / 0 |
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00014428 | 2 / 2 |
| O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00006976 | 0 / 0 |
| P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00006971 | 0 / 3 |
| P14555 | Phospholipase A2, membrane associated | Enzyme | C00006971 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #202300 | Adrenocortical carcinoma, hereditary; adcc |
P04637
|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #609135 | Aplastic anemia |
O14746
|
| #613546 | Aromatase deficiency |
P11511
|
| #139300 | Aromatase excess syndrome; aexs |
P11511
|
| #608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
| #208900 | Ataxia-telangiectasia; at |
Q13315
|
| #614740 | Basal cell carcinoma, susceptibility to, 7; bcc7 |
P04637
|
| #614490 | Blood group, junior system; jr |
Q9UNQ0
|
| %606641 | Body mass index; bmi |
P37231
|
| #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
|
| #114500 | Colorectal cancer; crc |
P18054
P84022 |
| #127750 | Dementia, lewy body; dlb |
P37840
|
| #119900 | Digital clubbing, isolated congenital |
P15428
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #613989 | Dyskeratosis congenita, autosomal dominant, 2; dkca2 |
O14746
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #133239 | Esophageal cancer |
P04637
P18054 |
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #137800 | Glioma susceptibility 1; glm1 |
O75874
P37231 |
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
| #612244 | Inflammatory bowel disease 13; ibd13 |
P08183
|
| #151623 | Li-fraumeni syndrome 1; lfs1 |
P04637
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #604367 | Lipodystrophy, familial partial, type 3; fpld3 |
P37231
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #211980 | Lung cancer |
P04637
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #615134 | Melanoma, cutaneous malignant, susceptibility to, 9; cmm9 |
O14746
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
| #257200 | Niemann-pick disease, type a |
P17405
|
| #607616 | Niemann-pick disease, type b |
P17405
|
| #601665 | Obesity |
P37231
|
| #166350 | Osseous heteroplasia, progressive; poh |
P63092
|
| #260500 | Papilloma of choroid plexus; cpp |
P04637
|
| #168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
| #605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
P37840 |
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #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
|
| #614742 | Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1 |
O14746
|
| #178500 | Pulmonary fibrosis, idiopathic; ipf |
O14746
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| #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
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #275355 | Squamous cell carcinoma, head and neck; hnscc |
P04637
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 |
Q9UNQ0
|
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
| #278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
| KEGG | name | UniProt |
|---|---|---|
| H00033 | Adrenal carcinoma |
O00255
(related)
P04637 (related) |
| H00034 | Carcinoid |
O00255
(related)
|
| H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
| H00246 | Primary hyperparathyroidism |
O00255
(related)
|
| H01102 | Pituitary adenomas |
O00255
(related)
|
| H00764 | Cri du chat syndrome |
O14746
(related)
|
| H01132 | Aplastic anemia (AA) |
O14746
(related)
|
| H01299 | Idiopathic pulmonary fibrosis |
O14746
(related)
|
| H00022 | Bladder cancer |
O14746
(marker)
P04637 (related) |
| H00024 | Prostate cancer |
O14746
(marker)
|
| H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
| H00082 | Graves' disease |
P01215
(marker)
|
| H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
| 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)
|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
P37840 (related) |
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(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)
|
| H00016 | Oral cancer |
P04637
(related)
P04637 (marker) |
| H00017 | Esophageal cancer |
P04637
(related)
P04637 (marker) |
| H00018 | Gastric cancer |
P04637
(related)
|
| H00019 | Pancreatic cancer |
P04637
(related)
P04637 (marker) |
| H00020 | Colorectal cancer |
P04637
(related)
P04637 (marker) |
| H00025 | Penile cancer |
P04637
(related)
P04637 (marker) |
| 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)
P37231 (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)
|
| 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)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (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)
|
| H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P11511
(related)
|
| H00794 | Aromatase excess syndrome |
P11511
(related)
|
| H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
| H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
| H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
| H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
| H00409 | Type II diabetes mellitus |
P37231
(related)
|
| H00057 | Parkinson's disease (PD) |
P37840
(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)
|
| H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
| H00094 | DNA repair defects |
Q13315
(related)
|
| H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|
| H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
| H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
| H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|
| H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|