Species

KNApSAcK Entry

Organism name Prunus serotina
Genus Prunus
Family Rosaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Prunus serotina
Linked NCBI taxonomy ID 23207
Linked level species

Family

Family in NCBI taxonomy Rosaceae
ID 3745

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Natural Activity

List (46)

Species Activity
Prunus serotina Ehrh. Analgesic
Prunus serotina Ehrh. Analgesic
Prunus serotina Ehrh. Antidiarrheal
Prunus serotina Ehrh. Antidiarrheal
Prunus serotina Ehrh. Antiinflammatory
Prunus serotina Ehrh. Antiinflammatory
Prunus serotina Ehrh. Antiproliferant
Prunus serotina Ehrh. Antiseptic
Prunus serotina Ehrh. Antiseptic
Prunus serotina Ehrh. Antispasmodic
Prunus serotina Ehrh. Antispasmodic
Prunus serotina Ehrh. Antitussive
Prunus serotina Ehrh. Antitussive
Prunus serotina Ehrh. Anxiolytic
Prunus serotina Ehrh. Apoptotic
Prunus serotina Ehrh. Astringent
Prunus serotina Ehrh. Astringent
Prunus serotina Ehrh. Chemopreventive
Prunus serotina Ehrh. Cyanogenic
Prunus serotina Ehrh. Cyanogenic
Prunus serotina Ehrh. Decongestant
Prunus serotina Ehrh. Decongestant
Prunus serotina Ehrh. Depurative
Prunus serotina Ehrh. Depurative
Prunus serotina Ehrh. Digestive
Prunus serotina Ehrh. Digestive
Prunus serotina Ehrh. Expectorant
Prunus serotina Ehrh. Expectorant
Prunus serotina Ehrh. Gastrostimulant
Prunus serotina Ehrh. Gastrostimulant
Prunus serotina Ehrh. Hematonic
Prunus serotina Ehrh. Hematonic
Prunus serotina Ehrh. Narcotic
Prunus serotina Ehrh. Narcotic
Prunus serotina Ehrh. Pectoral
Prunus serotina Ehrh. Pectoral
Prunus serotina Ehrh. Poison
Prunus serotina Ehrh. Poison
Prunus serotina Ehrh. Sedative
Prunus serotina Ehrh. Sedative
Prunus serotina Ehrh. Tonic
Prunus serotina Ehrh. Tonic
Prunus serotina Ehrh. Tranquilizer
Prunus serotina Ehrh. Tranquilizer
Prunus serotina Ehrh. Vermifuge
Prunus serotina Ehrh. Vermifuge

Metabolite list (2)

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
C00001437 External link 512 Amygdalin
/ (R)-Amygdalin
CHEMBL515712
CHEMBL461727
CHEMBL1967951
CHEMBL2007233
D000678
92 / 37 / 31 No. 128 No. 72
C00002499 External link 512 Scopoletin
CHEMBL71851
D012603
48 / 37 / 34 9 / 0 No. 864 No. 25

Human Protein / Gene in interactions

131 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001437 C00002499 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001437 C00002499 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001437 C00002499 1 / 1
P22303 Acetylcholinesterase Hydrolase C00001437 C00002499 1 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001437 C00002499 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001437 C00002499 0 / 1
P00918 Carbonic anhydrase 2 Lyase C00001437 C00002499 1 / 2
P29466 Caspase-1 C14 C00001437 C00002499 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00001437 C00002499 0 / 3
Q16790 Carbonic anhydrase 9 Lyase C00002499 0 / 1
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00001437 2 / 2
P08246 Neutrophil elastase S1A C00001437 2 / 1
P33765 Adenosine receptor A3 Adenosine receptor C00001437 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00001437 0 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00001437 0 / 0
P04062 Glucosylceramidase Enzyme C00002499 6 / 4
P10253 Lysosomal alpha-glucosidase Hydrolase C00002499 1 / 1
P43166 Carbonic anhydrase 7 Lyase C00002499 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00001437 0 / 0
P17252 Protein kinase C alpha type Alpha C00001437 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00001437 0 / 0
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00002499 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00001437 2 / 2
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00002499 0 / 0
Q8N1Q1 Carbonic anhydrase 13 Lyase C00002499 0 / 0
P55789 FAD-linked sulfhydryl oxidase ALR Enzyme C00002499 1 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00002499 1 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002499 0 / 0
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00001437 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00001437 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00001437 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00001437 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00001437 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00001437 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00001437 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00001437 0 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00001437 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00001437 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00001437 0 / 0
Q99700 Ataxin-2 Unclassified protein C00002499 1 / 1
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00001437 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00001437 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00001437 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00001437 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00001437 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00001437 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00001437 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00001437 0 / 0
P01730 T-cell surface glycoprotein CD4 Surface antigen C00001437 1 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00001437 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00001437 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00001437 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002499 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00002499 1 / 2
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00001437 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00002499 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002499 0 / 0
O75496 Geminin Unclassified protein C00002499 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00002499 0 / 0
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00002499 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00001437 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00001437 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00001437 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00001437 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00001437 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00001437 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00001437 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00001437 0 / 0
P15121 Aldose reductase Enzyme C00002499 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00001437 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00001437 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00001437 1 / 0
P00915 Carbonic anhydrase 1 Lyase C00002499 0 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00001437 0 / 0
P08311 Cathepsin G S1A C00001437 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00001437 1 / 0
P03956 Interstitial collagenase M10A C00001437 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00001437 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00002499 7 / 3
Q04206 Transcription factor p65 Transcription Factor C00002499 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00001437 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00001437 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00001437 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00001437 0 / 0
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00001437 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00001437 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00001437 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00001437 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00001437 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00001437 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00001437 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00001437 0 / 0
P06280 Alpha-galactosidase A Enzyme C00002499 1 / 1
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00001437 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00001437 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00001437 2 / 1
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00002499 0 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00001437 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002499 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002499 2 / 2
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00002499 0 / 0
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00002499 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00001437 0 / 0
P03372 Estrogen receptor NR3A1 C00001437 1 / 1
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00001437 1 / 0
O75795 UDP-glucuronosyltransferase 2B17 Enzyme C00002499 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00001437 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00001437 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00001437 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00001437 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00001437 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00001437 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00001437 0 / 0
Q00796 Sorbitol dehydrogenase Enzyme C00002499 0 / 0
P55210 Caspase-7 C14 C00002499 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00002499 0 / 0
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00002499 3 / 0
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00001437 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00002499 5 / 1
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00001437 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00001437 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00001437 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00001437 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00001437 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00001437 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00001437 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002499 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00002499 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002499 0 / 0
O00255 Menin Unclassified protein C00002499 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002499 1 / 2

9 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00002499
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002499
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00002499
54578 UGT1A6, GNT1, HLUGP, HLUGP1, UDPGT, UDPGT_1-6, UGT1, UGT1A6S, UGT1F UDP glucuronosyltransferase 1 family, polypeptide A6 (EC:2.4.1.17) C00002499
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002499
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) C00002499
54600 UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) C00002499
7366 UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) C00002499
7508 XPC, RAD4, XP3, XPCC xeroderma pigmentosum, complementation group C C00002499

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (70)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#103780 Alcohol dependence P08172
P14416
P31645
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#612560 Bone mineral density quantitative trait locus 12; bmnd12 O75795
#300615 Brunner syndrome P21397
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#162800 Cyclic neutropenia P08246
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#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
#143500 Gilbert syndrome P22309
P22310
#137800 Glioma susceptibility 1; glm1 P04626
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#143860 Hyperchlorhidrosis, isolated O43570
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#603932 Intervertebral disc disease; idd P14780
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04626
#608516 Major depressive disorder; mdd P08172
#174800 Mccune-albright syndrome; mas P63092
#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
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#126200 Multiple sclerosis, susceptibility to; ms P08575
#159900 Myoclonic dystonia P14416
#613076 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay P55789
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#613949 Okt4 epitope deficiency P01730
#604715 Orthostatic intolerance P23975
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#168600 Parkinson disease, late-onset; pd P04062
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#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
#607276 Resting heart rate, variation in P08588
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#190300 Tremor, hereditary essential, 1; etm1 P35462
#610379 West nile virus, susceptibility to P51681
#278300 Xanthinuria, type i P47989
#112100 Yt blood group antigen P22303

KEGG DISEASE (56)

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)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
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)
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)
H00125 Fabry disease P06280 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H01205 Coumarin resistance P11712 (related)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00548 Brunner syndrome P21397 (related)
H00208 Hyperbilirubinemia P22309 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00192 Xanthinuria P47989 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
Q99714 (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)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)