| Organism name | Spondias mangifera | 
|---|---|
| Genus | Spondias | 
| Family | Anacardiaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Spondias | 
|---|---|
| Linked NCBI taxonomy ID | 43860 | 
| Linked level | genus | 
| Family in NCBI taxonomy | Anacardiaceae | 
|---|---|
| ID | 4011 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | rosids | 
|---|---|
| ID | 71275 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| 
                        C00002218
                        
                           | 
                      
                        Cytisine
                         / (-)-Cytisine  | 
                      
                        CHEMBL47039
                         CHEMBL497939 CHEMBL1628606  | 
                      
                        C004712
                         | 
                      27 / 36 / 33 | 6 / 1 | No. 376 | No. 3 | 
                         
                       | 
                    
| 
                        C00001361
                        
                           | 
                      
                        Glycine
                         | 
                      
                        CHEMBL773
                         | 
                      95 / 37 / 32 | No. 3932 | 
                         
                       | 
                    
| accession | description | class description | KNApSAcK metabolite in interactions | 
                          # of diseases
                           (OMIM / KEGG)  | 
                      
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001361 C00002218 | 1 / 0 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001361 C00002218 | 0 / 1 | 
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001361 C00002218 | 1 / 1 | 
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001361 C00002218 | 0 / 0 | 
| P36544 | Neuronal acetylcholine receptor subunit alpha-7 | CHRN alpha | C00001361 C00002218 | 0 / 0 | 
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001361 C00002218 | 0 / 1 | 
| P03372 | Estrogen receptor | NR3A1 | C00001361 | 1 / 1 | 
| Q16539 | Mitogen-activated protein kinase 14 | p38 | C00001361 | 0 / 0 | 
| P49146 | Neuropeptide Y receptor type 2 | Neuropeptide Y receptor | C00001361 | 0 / 0 | 
| P46059 | Solute carrier family 15 member 1 | Dipeptide | C00001361 | 0 / 0 | 
| P04062 | Glucosylceramidase | Enzyme | C00002218 | 6 / 4 | 
| P29466 | Caspase-1 | C14 | C00001361 | 0 / 0 | 
| P17252 | Protein kinase C alpha type | Alpha | C00001361 | 0 / 0 | 
| P27361 | Mitogen-activated protein kinase 3 | Erk | C00001361 | 0 / 0 | 
| P14780 | Matrix metalloproteinase-9 | M10A | C00001361 | 2 / 2 | 
| P02545 | Prelamin-A/C | Unclassified protein | C00002218 | 11 / 10 | 
| P23415 | Glycine receptor subunit alpha-1 | GLR alpha | C00001361 | 1 / 1 | 
| P00918 | Carbonic anhydrase 2 | Lyase | C00001361 | 1 / 2 | 
| P07550 | Beta-2 adrenergic receptor | Adrenergic receptor | C00001361 | 0 / 1 | 
| P21397 | Amine oxidase [flavin-containing] A | Oxidoreductase | C00001361 | 1 / 1 | 
| P25021 | Histamine H2 receptor | Histamine receptor | C00001361 | 0 / 0 | 
| P35367 | Histamine H1 receptor | Histamine receptor | C00001361 | 0 / 0 | 
| Q01959 | Sodium-dependent dopamine transporter | Dopamine | C00001361 | 1 / 0 | 
| P08912 | Muscarinic acetylcholine receptor M5 | Acetylcholine receptor | C00001361 | 0 / 0 | 
| P18825 | Alpha-2C adrenergic receptor | Adrenergic receptor | C00001361 | 0 / 0 | 
| P13945 | Beta-3 adrenergic receptor | Adrenergic receptor | C00001361 | 0 / 0 | 
| P25024 | C-X-C chemokine receptor type 1 | CXC chemokine receptor | C00001361 | 0 / 0 | 
| P06241 | Tyrosine-protein kinase Fyn | Src | C00001361 | 0 / 0 | 
| Q08209 | Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform | Ser_Thr | C00001361 | 0 / 0 | 
| P08246 | Neutrophil elastase | S1A | C00001361 | 2 / 1 | 
| P30926 | Neuronal acetylcholine receptor subunit beta-4 | CHRN beta | C00002218 | 0 / 0 | 
| P32297 | Neuronal acetylcholine receptor subunit alpha-3 | CHRN alpha | C00002218 | 1 / 0 | 
| Q07001 | Acetylcholine receptor subunit delta | CHRN delta | C00002218 | 3 / 2 | 
| P43681 | Neuronal acetylcholine receptor subunit alpha-4 | CHRN alpha | C00002218 | 1 / 1 | 
| P07510 | Acetylcholine receptor subunit gamma | CHRN gamma | C00002218 | 2 / 1 | 
| P17787 | Neuronal acetylcholine receptor subunit beta-2 | CHRN beta | C00002218 | 1 / 1 | 
| P02708 | Acetylcholine receptor subunit alpha | CHRN alpha | C00002218 | 3 / 2 | 
| P11230 | Acetylcholine receptor subunit beta | CHRN beta | C00002218 | 2 / 1 | 
| P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00001361 | 1 / 8 | 
| P14416 | D(2) dopamine receptor | Dopamine receptor | C00001361 | 2 / 0 | 
| P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00001361 | 0 / 0 | 
| P37288 | Vasopressin V1a receptor | Vasopressin and oxytocin receptor | C00001361 | 0 / 0 | 
| P41145 | Kappa-type opioid receptor | Opioid receptor | C00001361 | 0 / 0 | 
| Q9Y271 | Cysteinyl leukotriene receptor 1 | Leukotriene receptor | C00001361 | 0 / 0 | 
| P29274 | Adenosine receptor A2a | Adenosine receptor | C00001361 | 0 / 0 | 
| P25929 | Neuropeptide Y receptor type 1 | Neuropeptide Y receptor | C00001361 | 0 / 0 | 
| P50052 | Type-2 angiotensin II receptor | Angiotensin receptor | C00001361 | 1 / 1 | 
| P17948 | Vascular endothelial growth factor receptor 1 | Vegfr | C00001361 | 0 / 0 | 
| P41968 | Melanocortin receptor 3 | Melanocortin receptor | C00001361 | 1 / 0 | 
| P11509 | Cytochrome P450 2A6 | Cytochrome P450 2A6 | C00001361 | 0 / 0 | 
| O75496 | Geminin | Unclassified protein | C00002218 | 0 / 0 | 
| P04035 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase | Oxidoreductase | C00001361 | 0 / 0 | 
| P08913 | Alpha-2A adrenergic receptor | Adrenergic receptor | C00001361 | 0 / 0 | 
| P21917 | D(4) dopamine receptor | Dopamine receptor | C00001361 | 0 / 0 | 
| P30988 | Calcitonin receptor | Calcitonin receptor | C00001361 | 0 / 0 | 
| P35462 | D(3) dopamine receptor | Dopamine receptor | C00001361 | 1 / 0 | 
| P41143 | Delta-type opioid receptor | Opioid receptor | C00001361 | 0 / 0 | 
| P46098 | 5-hydroxytryptamine receptor 3A | NS | C00001361 | 0 / 0 | 
| Q92731 | Estrogen receptor beta | NR3A2 | C00001361 | 0 / 1 | 
| P41595 | 5-hydroxytryptamine receptor 2B | Serotonin receptor | C00001361 | 0 / 0 | 
| P25101 | Endothelin-1 receptor | Endothelin receptor | C00001361 | 0 / 0 | 
| P30411 | B2 bradykinin receptor | Bradykinin receptor | C00001361 | 0 / 0 | 
| P32245 | Melanocortin receptor 4 | Melanocortin receptor | C00001361 | 1 / 0 | 
| P32238 | Cholecystokinin receptor type A | Cholecystokinin receptor | C00001361 | 0 / 0 | 
| P08311 | Cathepsin G | S1A | C00001361 | 0 / 0 | 
| Q99720 | Sigma non-opioid intracellular receptor 1 | Membrane receptor | C00001361 | 1 / 0 | 
| P03956 | Interstitial collagenase | M10A | C00001361 | 0 / 1 | 
| P32241 | Vasoactive intestinal polypeptide receptor 1 | Vasoactive intestinal peptide receptor | C00001361 | 0 / 0 | 
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002218 | 0 / 0 | 
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00002218 | 0 / 0 | 
| P04150 | Glucocorticoid receptor | NR3C1 | C00001361 | 0 / 1 | 
| P08172 | Muscarinic acetylcholine receptor M2 | Acetylcholine receptor | C00001361 | 2 / 0 | 
| P11229 | Muscarinic acetylcholine receptor M1 | Acetylcholine receptor | C00001361 | 0 / 0 | 
| P21554 | Cannabinoid receptor 1 | Cannabinoid receptor | C00001361 | 0 / 0 | 
| P31645 | Sodium-dependent serotonin transporter | Serotonin | C00001361 | 2 / 0 | 
| P04626 | Receptor tyrosine-protein kinase erbB-2 | TK tyrosine-protein kinase EGFR subfamily | C00001361 | 5 / 9 | 
| P20309 | Muscarinic acetylcholine receptor M3 | Acetylcholine receptor | C00001361 | 1 / 0 | 
| P21452 | Substance-K receptor | Neurokinin receptor | C00001361 | 0 / 0 | 
| P51679 | C-C chemokine receptor type 4 | CC chemokine receptor | C00001361 | 0 / 0 | 
| P51681 | C-C chemokine receptor type 5 | CC chemokine receptor | C00001361 | 3 / 0 | 
| P50406 | 5-hydroxytryptamine receptor 6 | Serotonin receptor | C00001361 | 0 / 0 | 
| Q12809 | Potassium voltage-gated channel subfamily H member 2 | KCNH, Kv10-12.x (Ether-a-go-go) | C00001361 | 2 / 2 | 
| P41597 | C-C chemokine receptor type 2 | CC chemokine receptor | C00001361 | 1 / 0 | 
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00001361 | 0 / 0 | 
| P08575 | Receptor-type tyrosine-protein phosphatase C | Enzyme | C00001361 | 2 / 1 | 
| P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00001361 | 0 / 3 | 
| O76074 | cGMP-specific 3',5'-cyclic phosphodiesterase | PDE_5A | C00001361 | 0 / 0 | 
| P33765 | Adenosine receptor A3 | Adenosine receptor | C00001361 | 0 / 0 | 
| P08588 | Beta-1 adrenergic receptor | Adrenergic receptor | C00001361 | 1 / 0 | 
| P22303 | Acetylcholinesterase | Hydrolase | C00001361 | 1 / 0 | 
| P28223 | 5-hydroxytryptamine receptor 2A | Serotonin receptor | C00001361 | 0 / 0 | 
| P28335 | 5-hydroxytryptamine receptor 2C | Serotonin receptor | C00001361 | 0 / 0 | 
| P35372 | Mu-type opioid receptor | Opioid receptor | C00001361 | 0 / 0 | 
| P08173 | Muscarinic acetylcholine receptor M4 | Acetylcholine receptor | C00001361 | 0 / 0 | 
| P25103 | Substance-P receptor | Neurokinin receptor | C00001361 | 0 / 0 | 
| P25105 | Platelet-activating factor receptor | PAF receptor | C00001361 | 0 / 0 | 
| P33032 | Melanocortin receptor 5 | Melanocortin receptor | C00001361 | 0 / 0 | 
| P21728 | D(1A) dopamine receptor | Dopamine receptor | C00001361 | 0 / 0 | 
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00002218 | 0 / 0 | 
| P05181 | Cytochrome P450 2E1 | Cytochrome P450 2E1 | C00001361 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00002218 | 4 / 3 | 
| Q7Z2H8 | Proton-coupled amino acid transporter 1 | Unclassified protein | C00001361 | 0 / 0 | 
| P23975 | Sodium-dependent noradrenaline transporter | Norepinephrine | C00001361 | 1 / 1 | 
| P25100 | Alpha-1D adrenergic receptor | Adrenergic receptor | C00001361 | 0 / 0 | 
| P30542 | Adenosine receptor A1 | Adenosine receptor | C00001361 | 0 / 0 | 
| P18089 | Alpha-2B adrenergic receptor | Adrenergic receptor | C00001361 | 0 / 0 | 
| P24557 | Thromboxane-A synthase | Cytochrome P450 5A1 | C00001361 | 1 / 1 | 
| P06239 | Tyrosine-protein kinase Lck | Src | C00001361 | 0 / 1 | 
| P25025 | C-X-C chemokine receptor type 2 | CXC chemokine receptor | C00001361 | 0 / 0 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002218 | 0 / 0 | 
| O00255 | Menin | Unclassified protein | C00002218 | 2 / 5 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002218 | 1 / 2 | 
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00002218 | 0 / 1 | 
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00002218 | 1 / 4 | 
| Q15822 | Neuronal acetylcholine receptor subunit alpha-2 | CHRN alpha | C00002218 | 1 / 1 | 
| Q05BR4 | SLC16A10 protein | Unclassified protein | C00001361 | 0 / 0 | 
| gene | gene name | gene description | KNApSAcK metabolite in interactions | 
|---|---|---|---|
| 1135 | CHRNA2 | cholinergic receptor, nicotinic, alpha 2 (neuronal) | 
                          C00002218
                           | 
                      
| 1136 | CHRNA3, LNCR2, NACHRA3, PAOD2 | cholinergic receptor, nicotinic, alpha 3 (neuronal) | 
                          C00002218
                           | 
                      
| 1137 | CHRNA4, BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4 | cholinergic receptor, nicotinic, alpha 4 (neuronal) | 
                          C00002218
                           | 
                      
| 1139 | CHRNA7, CHRNA7-2, NACHRA7 | cholinergic receptor, nicotinic, alpha 7 (neuronal) | 
                          C00002218
                           | 
                      
| 1141 | CHRNB2, EFNL3, nAChRB2 | cholinergic receptor, nicotinic, beta 2 (neuronal) | 
                          C00002218
                           | 
                      
| 1143 | CHRNB4 | cholinergic receptor, nicotinic, beta 4 (neuronal) | 
                          C00002218
                           | 
                      
| OMIM | preferred title | UniProt | 
|---|---|---|
| #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
                             | 
                        
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a | 
                            P02545
                             | 
                        
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism | 
                            P02545
                             | 
                        
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 | 
                            P02545
                             | 
                        
| #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
                             | 
                        
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 | 
                            P02545
                             | 
                        
| #600513 | Epilepsy, nocturnal frontal lobe, 1; enfl1 | 
                            P43681
                             | 
                        
| #605375 | Epilepsy, nocturnal frontal lobe, 3; enfl3 | 
                            P17787
                             | 
                        
| #610353 | Epilepsy, nocturnal frontal lobe, 4; enfl4 | 
                            Q15822
                             | 
                        
| #615363 | Estrogen resistance; estrr | 
                            P03372
                             | 
                        
| #600274 | Frontotemporal dementia; ftd | 
                            P10636
                             | 
                        
| #613659 | Gastric cancer | 
                            P04626
                             | 
                        
| #137215 | Gastric cancer, hereditary diffuse; hdgc | 
                            P04626
                             | 
                        
| #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
                             | 
                        
| #231095 | Ghosal hematodiaphyseal dysplasia; ghdd | 
                            P24557
                             | 
                        
| #137800 | Glioma susceptibility 1; glm1 | 
                            P04626
                             | 
                        
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay | 
                            Q03164
                             | 
                        
| #610140 | Heart-hand syndrome, slovenian type | 
                            P02545
                             | 
                        
| #609423 | Human immunodeficiency virus type 1, susceptibility to | 
                            P41597
                             P51681  | 
                        
| #176670 | Hutchinson-gilford progeria syndrome; hgps | 
                            P02545
                             | 
                        
| #149400 | Hyperekplexia, hereditary 1; hkpx1 | 
                            P23415
                             | 
                        
| #145000 | Hyperparathyroidism 1; hrpt1 | 
                            O00255
                             | 
                        
| #603932 | Intervertebral disc disease; idd | 
                            P14780
                             | 
                        
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 | 
                            P02545
                             | 
                        
| #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
                             | 
                        
| %300852 | Mental retardation, x-linked 88; mrx88 | 
                            P50052
                             | 
                        
| #613073 | Metaphyseal anadysplasia 2; mandp2 | 
                            P14780
                             | 
                        
| #131100 | Multiple endocrine neoplasia, type i; men1 | 
                            O00255
                             | 
                        
| #265000 | Multiple pterygium syndrome, escobar variant; evmps | 
                            P07510
                             | 
                        
| #253290 | Multiple pterygium syndrome, lethal type; lmps | 
                            P02708
                             P07510 Q07001  | 
                        
| #126200 | Multiple sclerosis, susceptibility to; ms | 
                            P08575
                             | 
                        
| #613205 | Muscular dystrophy, congenital, lmna-related | 
                            P02545
                             | 
                        
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b | 
                            P02545
                             | 
                        
| #608931 | Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency | 
                            P11230
                             | 
                        
| #608930 | Myasthenic syndrome, congenital, fast-channel | 
                            P02708
                             Q07001  | 
                        
| #601462 | Myasthenic syndrome, congenital, slow-channel; sccms | 
                            P02708
                             P11230 Q07001  | 
                        
| #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
                             | 
                        
| #168600 | Parkinson disease, late-onset; pd | 
                            P04062
                             | 
                        
| #260540 | Parkinson-dementia syndrome | 
                            P10636
                             | 
                        
| #613135 | Parkinsonism-dystonia, infantile; pkdys | 
                            Q01959
                             | 
                        
| #172700 | Pick disease of brain | 
                            P10636
                             | 
                        
| #601399 | Platelet disorder, familial, with associated myeloid malignancy | 
                            Q01196
                             | 
                        
| #607276 | Resting heart rate, variation in | 
                            P08588
                             | 
                        
| #275210 | Restrictive dermopathy, lethal | 
                            P02545
                             | 
                        
| #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
                             | 
                        
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | 
                            P10636
                             | 
                        
| #190300 | Tremor, hereditary essential, 1; etm1 | 
                            P35462
                             | 
                        
| #610379 | West nile virus, susceptibility to | 
                            P51681
                             | 
                        
| #112100 | Yt blood group antigen | 
                            P22303
                             | 
                        
| KEGG | name | UniProt | 
|---|---|---|
| H00033 | Adrenal carcinoma | 
                            O00255
                            (related)
                             | 
                        
| H00034 | Carcinoid | 
                            O00255
                            (related)
                             | 
                        
| H00045 | Malignant islet cell carcinoma | 
                            O00255
                            (related)
                             | 
                        
| H00246 | Primary hyperparathyroidism | 
                            O00255
                            (related)
                             | 
                        
| H01102 | Pituitary adenomas | 
                            O00255
                            (related)
                             | 
                        
| 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)
                             | 
                        
| 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)
                             | 
                        
| H00770 | Congenital myasthenic syndrome | 
                            P02708
                            (related)
                             P11230 (related) Q07001 (related)  | 
                        
| H00986 | Multiple pterygium syndrome | 
                            P02708
                            (related)
                             P07510 (related) Q07001 (related)  | 
                        
| H00026 | Endometrial Cancer | 
                            P03372
                            (marker)
                             P04626 (related) Q92731 (marker)  | 
                        
| H00066 | Lewy body dementia (LBD) | 
                            P04062
                            (related)
                             | 
                        
| H00126 | Gaucher disease | 
                            P04062
                            (related)
                             | 
                        
| H00426 | Defects in the degradation of ganglioside | 
                            P04062
                            (related)
                             | 
                        
| H00810 | Progressive myoclonic epilepsy (PME) | 
                            P04062
                            (related)
                             | 
                        
| 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)
                             | 
                        
| H00058 | Amyotrophic lateral sclerosis (ALS) | 
                            P10636
                            (related)
                             | 
                        
| H00077 | Progressive supranuclear palsy (PSP) | 
                            P10636
                            (related)
                             | 
                        
| H00078 | Frontotemporal lobar degeneration (FTLD) | 
                            P10636
                            (related)
                             | 
                        
| H01205 | Coumarin resistance | 
                            P11712
                            (related)
                             | 
                        
| H00025 | Penile cancer | 
                            P14780
                            (related)
                             P35354 (related)  | 
                        
| H00479 | Metaphyseal dysplasias | 
                            P14780
                            (related)
                             | 
                        
| H00807 | Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) | 
                            P17787
                            (related)
                             P43681 (related) Q15822 (related)  | 
                        
| H00548 | Brunner syndrome | 
                            P21397
                            (related)
                             | 
                        
| H00769 | Hyperekplexia | 
                            P23415
                            (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)
                             | 
                        
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) | 
                            Q01196
                            (related)
                             Q01196 (marker) Q03164 (related) Q03164 (marker)  | 
                        
| H00003 | Acute myeloid leukemia (AML) | 
                            Q01196
                            (related)
                             Q01196 (marker) Q13951 (marker)  | 
                        
| H00004 | Chronic myeloid leukemia (CML) | 
                            Q01196
                            (related)
                             | 
                        
| H00978 | Thrombocytopenia (THC) | 
                            Q01196
                            (related)
                             | 
                        
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) | 
                            Q03164
                            (related)
                             | 
                        
| H00720 | Long QT syndrome | 
                            Q12809
                            (related)
                             | 
                        
| H00725 | Short QT syndrome | 
                            Q12809
                            (related)
                             |