association dataset threshold value standardized value Unspecified Visual Loss DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the metencephalon HPO Gene-Disease Associations 1.0 null Preexcitation Syndrome DisGeNET Gene-Disease Associations 1.0 null apnea HPO Gene-Disease Associations 1.0 null localized skin lesion HPO Gene-Disease Associations 1.0 null Sensorimotor Neuropathy DisGeNET Gene-Disease Associations 1.0 null vascular skin abnormality HPO Gene-Disease Associations 1.0 null cholerae GeneRIF Biological Term Annotations 1.0 null hypertension HPO Gene-Disease Associations 1.0 null abnormality of muscle morphology HPO Gene-Disease Associations 1.0 null Forgetful DisGeNET Gene-Phenotype Associations 1.0 null cholera GeneRIF Biological Term Annotations 1.0 null Simple Obesity DisGeNET Gene-Disease Associations 1.0 null primary GeneRIF Biological Term Annotations 1.0 null abnormality of the skin HPO Gene-Disease Associations 1.0 null abnormality of dental structure HPO Gene-Disease Associations 1.0 null Oxidative phosphorylation(Homo sapiens) WikiPathways Pathways 2014 1.0 null alitretinoin_rattus norvegicus_gpl85_liver b_gds2385 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null abnormality of the cardiovascular system HPO Gene-Disease Associations 1.0 null growth abnormality HPO Gene-Disease Associations 1.0 null KMS-12-PE Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 PMC5943339__F4 PFOCR Pathway Figure Associations 2023 1.0 null Abnormal Vision DisGeNET Gene-Phenotype Associations 1.0 null LN-18 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.63417 Proteinuria DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the lung HPO Gene-Disease Associations 1.0 null malformation of the heart and great vessels HPO Gene-Disease Associations 1.0 null SK-MEL-24 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.916601 Bipolar Disorder HuGE Navigator Gene-Phenotype Associations 1.0 null aplasia/hypoplasia of the cerebellum HPO Gene-Disease Associations 1.0 null abnormality of eye movement HPO Gene-Disease Associations 1.0 null Pancreatitis DisGeNET Gene-Disease Associations 1.0 null encephalomyopathy GeneRIF Biological Term Annotations 1.0 null aplasia/hypoplasia involving the central nervous system HPO Gene-Disease Associations 1.0 null abnormality of skeletal maturation HPO Gene-Disease Associations 1.0 null abnormal nerve conduction velocity HPO Gene-Disease Associations 1.0 null A-427 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 OKAJIMA Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -2.07082 Amaurosis DisGeNET Gene-Phenotype Associations 1.0 null egfr GeneRIF Biological Term Annotations 1.0 null abnormality of the pulmonary artery HPO Gene-Disease Associations 1.0 null arthrogryposis multiplex congenita HPO Gene-Disease Associations 1.0 null abnormality of the head HPO Gene-Disease Associations 1.0 null hsa-let-7b-5p MiRTarBase microRNA Targets 1.0 null Nystagmus DisGeNET Gene-Phenotype Associations 1.0 null Ataxia DisGeNET Gene-Phenotype Associations 1.0 null Hepatomegaly DisGeNET Gene-Phenotype Associations 1.0 null functional abnormality of the inner ear HPO Gene-Disease Associations 1.0 null abnormality of the nephron HPO Gene-Disease Associations 1.0 null Anoxia DisGeNET Gene-Phenotype Associations 1.0 null SNU-423 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.04602 NCI-H1395 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 intestine GeneRIF Biological Term Annotations 1.0 null episodes GeneRIF Biological Term Annotations 1.0 null optic GeneRIF Biological Term Annotations 1.0 null premature loss of teeth HPO Gene-Disease Associations 1.0 null MKN-45 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.38907 presence GeneRIF Biological Term Annotations 1.0 null Cerebral Calcification DisGeNET Gene-Phenotype Associations 1.0 null abnormality of adipose tissue HPO Gene-Disease Associations 1.0 null Prucalopride DeepCoverMOA Drug Mechanisms of Action -1.0 -0.21 abnormality of the middle ear HPO Gene-Disease Associations 1.0 null YAPC Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.942299 abnormality of the face HPO Gene-Disease Associations 1.0 null abnormality of the renal tubule HPO Gene-Disease Associations 1.0 null detected GeneRIF Biological Term Annotations 1.0 null phenotypic abnormality HPO Gene-Disease Associations 1.0 null Desipramine DeepCoverMOA Drug Mechanisms of Action -1.0 -0.48 colorectal cancer GAD Gene-Disease Associations 1.0 null respiratory electron transport chain GO Biological Process Annotations 2015 1.0 null cataract HPO Gene-Disease Associations 1.0 null Peripheral Demyelinating Neuropathy DisGeNET Gene-Disease Associations 1.0 null HCC1187 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.58879 oxidoreductase activity, acting on nad(p)h GO Molecular Function Annotations 2015 1.0 null cause GeneRIF Biological Term Annotations 1.0 null abnormality of the parathyroid gland HPO Gene-Disease Associations 1.0 null Tremor DisGeNET Gene-Phenotype Associations 1.0 null Respiratory chain complex I, mitochondrial CORUM Protein Complexes 1.0 null dominantly GeneRIF Biological Term Annotations 1.0 null even GeneRIF Biological Term Annotations 1.0 null abnormality of the immune system HPO Gene-Disease Associations 1.0 null Left Ventricular Hypertrophy DisGeNET Gene-Disease Associations 1.0 null aortic dilatation HPO Gene-Disease Associations 1.0 null nonsense GeneRIF Biological Term Annotations 1.0 null NCI-H2722 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.903653 abnormality of joint mobility HPO Gene-Disease Associations 1.0 null abnormality of the genitourinary system HPO Gene-Disease Associations 1.0 null Abnormality Of Retinal Pigmentation DisGeNET Gene-Phenotype Associations 1.0 null HS 746T Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -3.82124 abnormality of the skull HPO Gene-Disease Associations 1.0 null arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis GAD Gene-Disease Associations 1.0 null schizophrenia GeneRIF Biological Term Annotations 1.0 null Liver Carcinoma DisGeNET Gene-Disease Associations 1.0 null act GeneRIF Biological Term Annotations 1.0 null seizures HPO Gene-Disease Associations 1.0 null cellular_component GO Cellular Component Annotations 2015 1.0 null SNU-398 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 NCI-H1581 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.903653 m14453ga GeneRIF Biological Term Annotations 1.0 null Electroencephalogram Abnormal DisGeNET Gene-Phenotype Associations 1.0 null Respiratory chain complex I (holoenzyme), mitochondrial CORUM Protein Complexes 1.0 null samples GeneRIF Biological Term Annotations 1.0 null abnormal glucose homeostasis HPO Gene-Disease Associations 1.0 null sensorineural hearing impairment HPO Gene-Disease Associations 1.0 null HCC1482 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 number GeneRIF Biological Term Annotations 1.0 null hyperthyroidism HPO Gene-Disease Associations 1.0 null abnormality of the hypothalamus-pituitary axis HPO Gene-Disease Associations 1.0 null developmental regression HPO Gene-Disease Associations 1.0 null growth delay HPO Gene-Disease Associations 1.0 null morphological abnormality of the central nervous system HPO Gene-Disease Associations 1.0 null CAY10650 DeepCoverMOA Drug Mechanisms of Action 1.0 0.47 Multiple Lipomata DisGeNET Gene-Disease Associations 1.0 null PMC6781638__F4 PFOCR Pathway Figure Associations 2023 1.0 null chicken GeneRIF Biological Term Annotations 1.0 null carious teeth HPO Gene-Disease Associations 1.0 null lowlevel GeneRIF Biological Term Annotations 1.0 null emg abnormality HPO Gene-Disease Associations 1.0 null Wolff-Parkinson-White Syndrome DisGeNET Gene-Disease Associations 1.0 null cognitive impairment HPO Gene-Disease Associations 1.0 null OVMANA Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.36193 Obesity HuGE Navigator Gene-Phenotype Associations 1.0 null hypopigmentation of the skin HPO Gene-Disease Associations 1.0 null abdominal pain HPO Gene-Disease Associations 1.0 null Nonorganic Psychosis DisGeNET Gene-Disease Associations 1.0 null Vicriviroc DeepCoverMOA Drug Mechanisms of Action 1.0 0.26 respiratory GeneRIF Biological Term Annotations 1.0 null cardiomyopathy HPO Gene-Disease Associations 1.0 null alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease GAD Gene-Disease Associations 1.0 null Migalastat DeepCoverMOA Drug Mechanisms of Action -1.0 -0.32 ptosis HPO Gene-Disease Associations 1.0 null A-375 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.46316 cell part GO Cellular Component Annotations 2015 1.0 null abnormality of the retinal pigment epithelium HPO Gene-Disease Associations 1.0 null BCX 1470 DeepCoverMOA Drug Mechanisms of Action -1.0 -0.18 KURAMOCHI Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 abnormality of the aorta HPO Gene-Disease Associations 1.0 null major GeneRIF Biological Term Annotations 1.0 null Spasticity, Ctcae DisGeNET Gene-Phenotype Associations 1.0 null hypertrichosis HPO Gene-Disease Associations 1.0 null UACC-812 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 Diseases in Twins HuGE Navigator Gene-Phenotype Associations 1.0 null abnormal renal physiology HPO Gene-Disease Associations 1.0 null OVCAR433 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.942299 SK-MES-1 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.995046 total GeneRIF Biological Term Annotations 1.0 null Myelodysplastic Syndromes HuGE Navigator Gene-Phenotype Associations 1.0 null Rod-Cone Dystrophy DisGeNET Gene-Disease Associations 1.0 null Dental Caries DisGeNET Gene-Disease Associations 1.0 null Nyctalopia DisGeNET Gene-Disease Associations 1.0 null abnormality of muscle size HPO Gene-Disease Associations 1.0 null IU1 DeepCoverMOA Drug Mechanisms of Action 1.0 0.52 Death In Early Adulthood DisGeNET Gene-Phenotype Associations 1.0 null Delayed Puberty DisGeNET Gene-Phenotype Associations 1.0 null article GeneRIF Biological Term Annotations 1.0 null skeletal GeneRIF Biological Term Annotations 1.0 null NADH dehydrogenase subunit 5, C-terminal InterPro Predicted Protein Domain Annotations 1.0 null lebers GeneRIF Biological Term Annotations 1.0 null chinese GeneRIF Biological Term Annotations 1.0 null candidate GeneRIF Biological Term Annotations 1.0 null evidence GeneRIF Biological Term Annotations 1.0 null Breast Carcinoma DisGeNET Gene-Disease Associations 1.0 null abnormality of head or neck HPO Gene-Disease Associations 1.0 null feeding difficulties HPO Gene-Disease Associations 1.0 null including GeneRIF Biological Term Annotations 1.0 null Amyotrophic Lateral Sclerosis HuGE Navigator Gene-Phenotype Associations 1.0 null abnormality of forebrain morphology HPO Gene-Disease Associations 1.0 null hsa-miR-196b-5p MiRTarBase microRNA Targets 1.0 null bipolar disorder GAD Gene-Disease Associations 1.0 null abnormality of the pulmonary vasculature HPO Gene-Disease Associations 1.0 null tremor HPO Gene-Disease Associations 1.0 null Ophthalmoplegia DisGeNET Gene-Phenotype Associations 1.0 null cellular metabolic process GO Biological Process Annotations 2015 1.0 null abnormality of the cerebral vasculature HPO Gene-Disease Associations 1.0 null optic atrophy, hereditary, leber GAD Gene-Disease Associations 1.0 null Ataxia HuGE Navigator Gene-Phenotype Associations 1.0 null abnormality of peripheral nerve conduction HPO Gene-Disease Associations 1.0 null inherited GeneRIF Biological Term Annotations 1.0 null abnormality of the mouth HPO Gene-Disease Associations 1.0 null BL4797 (XPO6) NURSA Protein Complexes 1.0 null transcription GeneRIF Biological Term Annotations 1.0 null alitretinoin_rattus norvegicus_gpl85_lung_gds2385 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null neuropathy GeneRIF Biological Term Annotations 1.0 null abnormal facial expression HPO Gene-Disease Associations 1.0 null abnormality of body height HPO Gene-Disease Associations 1.0 null Prenatal Exposure Delayed Effects CTD Gene-Disease Associations 1.0 1.01966 features GeneRIF Biological Term Annotations 1.0 null mtdna GeneRIF Biological Term Annotations 1.0 null abnormality of carbohydrate metabolism/homeostasis HPO Gene-Disease Associations 1.0 null hereditary GeneRIF Biological Term Annotations 1.0 null decreased facial expression HPO Gene-Disease Associations 1.0 null Cardiac Conduction Abnormality DisGeNET Gene-Phenotype Associations 1.0 null myalgia HPO Gene-Disease Associations 1.0 null Abnormal Macular Morphology DisGeNET Gene-Phenotype Associations 1.0 null protein complex GO Cellular Component Annotations 2015 1.0 null abnormality of cerebral artery HPO Gene-Disease Associations 1.0 null abnormality of the intestine HPO Gene-Disease Associations 1.0 null abnormality of the eye HPO Gene-Disease Associations 1.0 null NCI-H2347 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.836485 Cataract DisGeNET Gene-Disease Associations 1.0 null organelle inner membrane GO Cellular Component Annotations 2015 1.0 null Hepatoblastoma DisGeNET Gene-Disease Associations 1.0 null Abnormal Visual Evoked Potential DisGeNET Gene-Phenotype Associations 1.0 null Acidosis, Lactic DisGeNET Gene-Phenotype Associations 1.0 null KMS-26 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 Constipation DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the glomerulus HPO Gene-Disease Associations 1.0 null hypertrophic cardiomyopathy HPO Gene-Disease Associations 1.0 null sensory neuropathy HPO Gene-Disease Associations 1.0 null abnormal renal morphology HPO Gene-Disease Associations 1.0 null Malignant Neoplasm DisGeNET Gene-Disease Associations 1.0 null night blindness HPO Gene-Disease Associations 1.0 null arrhythmia HPO Gene-Disease Associations 1.0 null Sensorineural Hearing Loss, Bilateral DisGeNET Gene-Disease Associations 1.0 null related GeneRIF Biological Term Annotations 1.0 null nd4 GeneRIF Biological Term Annotations 1.0 null Mitochondrial Encephalomyopathies DisGeNET Gene-Disease Associations 1.0 null neoplasm HPO Gene-Disease Associations 1.0 null Renal Insufficiency DisGeNET Gene-Disease Associations 1.0 null variation GeneRIF Biological Term Annotations 1.0 null Molindone DeepCoverMOA Drug Mechanisms of Action -1.0 -0.3 acidosis GeneRIF Biological Term Annotations 1.0 null abnormality of the globe HPO Gene-Disease Associations 1.0 null cardiomyopathy GeneRIF Biological Term Annotations 1.0 null DV-90 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.39753 Merrf Syndrome DisGeNET Gene-Disease Associations 1.0 null brain GeneRIF Biological Term Annotations 1.0 null abnormality of the adrenal glands HPO Gene-Disease Associations 1.0 null behavioral abnormality HPO Gene-Disease Associations 1.0 null abnormality of the abdomen HPO Gene-Disease Associations 1.0 null cytoplasmic part GO Cellular Component Annotations 2015 1.0 null frontal GeneRIF Biological Term Annotations 1.0 null effects GeneRIF Biological Term Annotations 1.0 null abnormality of the lens HPO Gene-Disease Associations 1.0 null Proton-conducting membrane transporter, N-terminal domain InterPro Predicted Protein Domain Annotations 1.0 null deleterious GeneRIF Biological Term Annotations 1.0 null Stroke DisGeNET Gene-Phenotype Associations 1.0 null brain very small HPO Gene-Disease Associations 1.0 null abnormal tendon morphology HPO Gene-Disease Associations 1.0 null Mitochondrial Respiratory Chain Defects DisGeNET Gene-Phenotype Associations 1.0 null migraine HPO Gene-Disease Associations 1.0 null SW 403 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 SK-MEL-5 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 one GeneRIF Biological Term Annotations 1.0 null Squamous Cell Carcinoma Of Lung DisGeNET Gene-Disease Associations 1.0 null nonsynonymous GeneRIF Biological Term Annotations 1.0 null onset HPO Gene-Disease Associations 1.0 null abnormality of the liver HPO Gene-Disease Associations 1.0 null Creutzfeldt-Jakob Disease, Sporadic DisGeNET Gene-Disease Associations 1.0 null Optic Atrophy HuGE Navigator Gene-Phenotype Associations 1.0 null isolated GeneRIF Biological Term Annotations 1.0 null Dystonia DisGeNET Gene-Phenotype Associations 1.0 null NCI-H716 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 nadh dehydrogenase activity GO Molecular Function Annotations 2015 1.0 null abnormality of body weight HPO Gene-Disease Associations 1.0 null mtnd1 GeneRIF Biological Term Annotations 1.0 null sudden central visual loss HPO Gene-Disease Associations 1.0 null Protruding Ear DisGeNET Gene-Phenotype Associations 1.0 null Osilodrostat DeepCoverMOA Drug Mechanisms of Action -1.0 -0.28 KNS-62 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 Apnea DisGeNET Gene-Phenotype Associations 1.0 null mode of inheritance HPO Gene-Disease Associations 1.0 null Muscle Spasticity DisGeNET Gene-Phenotype Associations 1.0 null Tropicamide DeepCoverMOA Drug Mechanisms of Action 1.0 0.26 lacking GeneRIF Biological Term Annotations 1.0 null atrophy/degeneration affecting the cerebrum HPO Gene-Disease Associations 1.0 null G-361 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.58879 several GeneRIF Biological Term Annotations 1.0 null papilledema HPO Gene-Disease Associations 1.0 null Anxiety DisGeNET Gene-Disease Associations 1.0 null cerebral cortical atrophy HPO Gene-Disease Associations 1.0 null families GeneRIF Biological Term Annotations 1.0 null ichthyosis HPO Gene-Disease Associations 1.0 null m13513ga GeneRIF Biological Term Annotations 1.0 null membrane part GO Cellular Component Annotations 2015 1.0 null abnormality of cell physiology HPO Gene-Disease Associations 1.0 null Gastroparesis DisGeNET Gene-Disease Associations 1.0 null Disease HuGE Navigator Gene-Phenotype Associations 1.0 null Abnormality Of Krebs Cycle Metabolism DisGeNET Gene-Phenotype Associations 1.0 null mitochondrial part GO Cellular Component Annotations 2015 1.0 null malabsorption HPO Gene-Disease Associations 1.0 null ophthalmoparesis HPO Gene-Disease Associations 1.0 null autism HPO Gene-Disease Associations 1.0 null skeletal muscle atrophy HPO Gene-Disease Associations 1.0 null NADH-plastoquinone oxidoreductase, chain 5 InterPro Predicted Protein Domain Annotations 1.0 null Tubulointerstitial Abnormality DisGeNET Gene-Disease Associations 1.0 null 888 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 supported GeneRIF Biological Term Annotations 1.0 null AZD 6482 DeepCoverMOA Drug Mechanisms of Action 1.0 0.7 Hyperthyroidism DisGeNET Gene-Disease Associations 1.0 null abnormality of calcium homeostasis HPO Gene-Disease Associations 1.0 null abnormality of neuronal migration HPO Gene-Disease Associations 1.0 null Eltrombopag DeepCoverMOA Drug Mechanisms of Action -1.0 -0.4 Cachexia DisGeNET Gene-Phenotype Associations 1.0 null position GeneRIF Biological Term Annotations 1.0 null HS 578T Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.45516 neoplasm of fatty tissue HPO Gene-Disease Associations 1.0 null abnormality of the myocardium HPO Gene-Disease Associations 1.0 null HCC2911 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 reduced consciousness/confusion HPO Gene-Disease Associations 1.0 null when GeneRIF Biological Term Annotations 1.0 null mRNA_SFPI1_19796622 ESCAPE Omics Signatures of Genes and Proteins for Stem Cells -1.0 null short attention span HPO Gene-Disease Associations 1.0 null functional respiratory abnormality HPO Gene-Disease Associations 1.0 null incoordination HPO Gene-Disease Associations 1.0 null abnormality of the vasculature HPO Gene-Disease Associations 1.0 null studied GeneRIF Biological Term Annotations 1.0 null biochemically GeneRIF Biological Term Annotations 1.0 null nadh dehydrogenase (ubiquinone) activity GO Molecular Function Annotations 2015 1.0 null Benethamine DeepCoverMOA Drug Mechanisms of Action -1.0 -0.35 abnormality of the gastrointestinal tract HPO Gene-Disease Associations 1.0 null SU-DHL-8 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.05809 Aortic Aneurysm DisGeNET Gene-Disease Associations 1.0 null A2780 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 2.22082 gastric cancer GAD Gene-Disease Associations 1.0 null HUH-7 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 abdominal symptom HPO Gene-Disease Associations 1.0 null flexion contracture HPO Gene-Disease Associations 1.0 null OVSAHO Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -2.24095 Electromyogram Abnormal DisGeNET Gene-Phenotype Associations 1.0 null abnormality of peripheral nerves HPO Gene-Disease Associations 1.0 null 4-Nitropiazthiole DeepCoverMOA Drug Mechanisms of Action 1.0 0.44 dna GeneRIF Biological Term Annotations 1.0 null hypoxia GeneRIF Biological Term Annotations 1.0 null KMS-28PE Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 abnormality of vision HPO Gene-Disease Associations 1.0 null coxi GeneRIF Biological Term Annotations 1.0 null pof - premature ovarian failure; primary ovarian insufficiency GAD Gene-Disease Associations 1.0 null hsa-miR-196a-5p MiRTarBase microRNA Targets 1.0 null abnormality of urine homeostasis HPO Gene-Disease Associations 1.0 null Myalgia DisGeNET Gene-Phenotype Associations 1.0 null Fatigue DisGeNET Gene-Phenotype Associations 1.0 null MFM-223 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.02111 Pinometostat DeepCoverMOA Drug Mechanisms of Action -1.0 -0.64 further GeneRIF Biological Term Annotations 1.0 null Heart Block DisGeNET Gene-Disease Associations 1.0 null unusually GeneRIF Biological Term Annotations 1.0 null eeg abnormality HPO Gene-Disease Associations 1.0 null Short Stature DisGeNET Gene-Phenotype Associations 1.0 null Chorea DisGeNET Gene-Phenotype Associations 1.0 null hypopituitarism HPO Gene-Disease Associations 1.0 null abnormal pattern of respiration HPO Gene-Disease Associations 1.0 null upregulated GeneRIF Biological Term Annotations 1.0 null aplasia/hypoplasia of the cerebrum HPO Gene-Disease Associations 1.0 null long qt syndrome GAD Gene-Disease Associations 1.0 null patient GeneRIF Biological Term Annotations 1.0 null Sensorineural Hearing Loss (Disorder) DisGeNET Gene-Disease Associations 1.0 null abnormality of the posterior segment of the eye HPO Gene-Disease Associations 1.0 null complexi GeneRIF Biological Term Annotations 1.0 null nephrotic syndrome HPO Gene-Disease Associations 1.0 null autistic behavior HPO Gene-Disease Associations 1.0 null molecular_function GO Molecular Function Annotations 2015 1.0 null HCT-15 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 2.22082 idiopathic GeneRIF Biological Term Annotations 1.0 null brain atrophy HPO Gene-Disease Associations 1.0 null Icthyosis DisGeNET Gene-Disease Associations 1.0 null severely GeneRIF Biological Term Annotations 1.0 null BT-483 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 hsa-miR-423-5p MiRTarBase microRNA Targets 1.0 null mitochondrial membrane part GO Cellular Component Annotations 2015 1.0 null Hemiparesis DisGeNET Gene-Phenotype Associations 1.0 null children GeneRIF Biological Term Annotations 1.0 null Decreased Nerve Conduction Velocity DisGeNET Gene-Phenotype Associations 1.0 null Olanzapine DeepCoverMOA Drug Mechanisms of Action 1.0 0.42 Focal T2 Hyperintense Basal Ganglia Lesion DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the optic disc HPO Gene-Disease Associations 1.0 null abnormality of the ear HPO Gene-Disease Associations 1.0 null A172 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.968512 contribute GeneRIF Biological Term Annotations 1.0 null largely GeneRIF Biological Term Annotations 1.0 null diethylstilbestrol_mus musculus_gpl6887_gse37969 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null abnormality of temperature regulation HPO Gene-Disease Associations 1.0 null structure GeneRIF Biological Term Annotations 1.0 null g11696a GeneRIF Biological Term Annotations 1.0 null Basimglurant DeepCoverMOA Drug Mechanisms of Action 1.0 0.37 Malabsorption, Ctcae DisGeNET Gene-Phenotype Associations 1.0 null proband GeneRIF Biological Term Annotations 1.0 null lactic GeneRIF Biological Term Annotations 1.0 null Nausea And Vomiting DisGeNET Gene-Phenotype Associations 1.0 null single-organism process GO Biological Process Annotations 2015 1.0 null mitochondrial membrane GO Cellular Component Annotations 2015 1.0 null screening GeneRIF Biological Term Annotations 1.0 null abnormality of the retina HPO Gene-Disease Associations 1.0 null Retinal Vascular Tortuosity DisGeNET Gene-Phenotype Associations 1.0 null RKO Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 virulence GeneRIF Biological Term Annotations 1.0 null OVCAR-5 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 2.22082 HCC1599 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.50851 Reduced Tendon Reflexes DisGeNET Gene-Phenotype Associations 1.0 null metabolic process GO Biological Process Annotations 2015 1.0 null hsa-let-7a-5p MiRTarBase microRNA Targets 1.0 null Spironolactone DeepCoverMOA Drug Mechanisms of Action -1.0 -0.33 abnormal muscle tone HPO Gene-Disease Associations 1.0 null abnormalities of the peripheral arteries HPO Gene-Disease Associations 1.0 null acid GeneRIF Biological Term Annotations 1.0 null electron transport chain GO Biological Process Annotations 2015 1.0 null primary adrenal insufficiency HPO Gene-Disease Associations 1.0 null Disturbance Of Consciousness DisGeNET Gene-Phenotype Associations 1.0 null abnormality of urine calcium concentration HPO Gene-Disease Associations 1.0 null Optic Atrophy DisGeNET Gene-Disease Associations 1.0 null decreased nerve conduction velocity HPO Gene-Disease Associations 1.0 null obvious GeneRIF Biological Term Annotations 1.0 null RAJI Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.23571 Malformations Of Cortical Development DisGeNET Gene-Disease Associations 1.0 null clinical modifier HPO Gene-Disease Associations 1.0 null adult testis HPM Cell Type and Tissue Protein Expression Profiles -1.0 -1.17092 MDA-MB-157 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -2.52574 under GeneRIF Biological Term Annotations 1.0 null Ventricular Dysfunction DisGeNET Gene-Phenotype Associations 1.0 null abnormal bleeding HPO Gene-Disease Associations 1.0 null Oxidative phosphorylation(Mus musculus) WikiPathways Pathways 2014 1.0 null Schizophrenia DisGeNET Gene-Disease Associations 1.0 null Maternally Inherited Leigh Syndrome DisGeNET Gene-Disease Associations 1.0 null Increased Serum Lactate DisGeNET Gene-Phenotype Associations 1.0 null mitochondrial GeneRIF Biological Term Annotations 1.0 null NCI-H2122 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 generalized abnormality of skin HPO Gene-Disease Associations 1.0 null course GeneRIF Biological Term Annotations 1.0 null Multiple Glomerular Cysts DisGeNET Gene-Phenotype Associations 1.0 null abnormal urinary electrolyte concentration HPO Gene-Disease Associations 1.0 null DOR 13 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.24592 NCI-H1092 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 2.22082 HT-1080 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.02111 goiter HPO Gene-Disease Associations 1.0 null mRNA_ESX1_19796622 ESCAPE Omics Signatures of Genes and Proteins for Stem Cells -1.0 null Central Visual Impairment DisGeNET Gene-Disease Associations 1.0 null Abnormality Of Mitochondrial Metabolism DisGeNET Gene-Phenotype Associations 1.0 null Scotoma DisGeNET Gene-Phenotype Associations 1.0 null Dyskinetic Syndrome DisGeNET Gene-Disease Associations 1.0 null lines GeneRIF Biological Term Annotations 1.0 null PMC5821407__F4 PFOCR Pathway Figure Associations 2023 1.0 null Electron Transport Chain(Homo sapiens) WikiPathways Pathways 2014 1.0 null Micronuclei, Chromosome-Defective CTD Gene-Disease Associations 1.0 1.01739 Spontaneous Hematomas DisGeNET Gene-Disease Associations 1.0 null Gait Ataxia DisGeNET Gene-Phenotype Associations 1.0 null abnormality of skin morphology HPO Gene-Disease Associations 1.0 null Multiple Sclerosis DisGeNET Gene-Disease Associations 1.0 null membrane GO Cellular Component Annotations 2015 1.0 null anorexia HPO Gene-Disease Associations 1.0 null NCI-H322T Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.98257 myopathy HPO Gene-Disease Associations 1.0 null respiratory activity following radiotherapy GAD Gene-Disease Associations 1.0 null hypothyroidism HPO Gene-Disease Associations 1.0 null cellular process GO Biological Process Annotations 2015 1.0 null leber optic atrophy HPO Gene-Disease Associations 1.0 null abnormality of the mitochondrion HPO Gene-Disease Associations 1.0 null Dwarfism DisGeNET Gene-Disease Associations 1.0 null variant GeneRIF Biological Term Annotations 1.0 null Diabetes Mellitus DisGeNET Gene-Disease Associations 1.0 null alitretinoin_rattus norvegicus_gpl85_gse3952 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null abnormality of vision evoked potentials HPO Gene-Disease Associations 1.0 null Segmental Peripheral Demyelination/Remyelination DisGeNET Gene-Phenotype Associations 1.0 null wpw GeneRIF Biological Term Annotations 1.0 null implicated GeneRIF Biological Term Annotations 1.0 null Respiratory chain complex I (beta subunit) mitochondrial CORUM Protein Complexes 1.0 null alters GeneRIF Biological Term Annotations 1.0 null Mirabegron DeepCoverMOA Drug Mechanisms of Action -1.0 -0.29 abnormality of higher mental function HPO Gene-Disease Associations 1.0 null Dilated Ventricles (Finding) DisGeNET Gene-Phenotype Associations 1.0 null Hypopigmented Skin Patch DisGeNET Gene-Phenotype Associations 1.0 null correlates GeneRIF Biological Term Annotations 1.0 null MDA-MB-231 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.836485 Attention Deficit Disorder DisGeNET Gene-Disease Associations 1.0 null elevated pulmonary artery pressure HPO Gene-Disease Associations 1.0 null anterior hypopituitarism HPO Gene-Disease Associations 1.0 null abnormal pyramidal signs HPO Gene-Disease Associations 1.0 null aortic dissection HPO Gene-Disease Associations 1.0 null Malabsorption DisGeNET Gene-Phenotype Associations 1.0 null causes GeneRIF Biological Term Annotations 1.0 null mtatp8 GeneRIF Biological Term Annotations 1.0 null Aneuploidy HuGE Navigator Gene-Phenotype Associations 1.0 null nd5 GeneRIF Biological Term Annotations 1.0 null abnormality of the musculature HPO Gene-Disease Associations 1.0 null Rupatadine DeepCoverMOA Drug Mechanisms of Action 1.0 0.74 paresthesia HPO Gene-Disease Associations 1.0 null Addison Disease DisGeNET Gene-Disease Associations 1.0 null L-Mimosine DeepCoverMOA Drug Mechanisms of Action -1.0 -0.33 ventriculomegaly HPO Gene-Disease Associations 1.0 null mtnd5 GeneRIF Biological Term Annotations 1.0 null blood GeneRIF Biological Term Annotations 1.0 null abnormal hair quantity HPO Gene-Disease Associations 1.0 null highly GeneRIF Biological Term Annotations 1.0 null contrast GeneRIF Biological Term Annotations 1.0 null single-organism metabolic process GO Biological Process Annotations 2015 1.0 null caused GeneRIF Biological Term Annotations 1.0 null OV56 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.849775 decreased body weight HPO Gene-Disease Associations 1.0 null SU-DHL-1 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.849775 4mu8C DeepCoverMOA Drug Mechanisms of Action -1.0 -0.28 abnormality of the urinary system HPO Gene-Disease Associations 1.0 null mitochondrial inner membrane GO Cellular Component Annotations 2015 1.0 null Episodic Respiratory Distress DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the cerebellum HPO Gene-Disease Associations 1.0 null ZINC6198410 DeepCoverMOA Drug Mechanisms of Action 1.0 0.31 Zaltoprofen DeepCoverMOA Drug Mechanisms of Action -1.0 -0.54 Hypoparathyroidism DisGeNET Gene-Disease Associations 1.0 null T84 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 andor GeneRIF Biological Term Annotations 1.0 null Cortical Visual Impairment DisGeNET Gene-Phenotype Associations 1.0 null headache HPO Gene-Disease Associations 1.0 null abnormality of globe location HPO Gene-Disease Associations 1.0 null MDA-MB-436 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.98257 Delayed Bone Age DisGeNET Gene-Phenotype Associations 1.0 null abnormality of skin adnexa HPO Gene-Disease Associations 1.0 null affected GeneRIF Biological Term Annotations 1.0 null Depression DisGeNET Gene-Disease Associations 1.0 null Intestinal Obstruction DisGeNET Gene-Disease Associations 1.0 null abnormal peripheral nervous system morphology HPO Gene-Disease Associations 1.0 null HCT-8 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 generation of precursor metabolites and energy GO Biological Process Annotations 2015 1.0 null abnormality of the thyroid gland HPO Gene-Disease Associations 1.0 null nd6 GeneRIF Biological Term Annotations 1.0 null deficiency GeneRIF Biological Term Annotations 1.0 null short stature HPO Gene-Disease Associations 1.0 null abnormality of the anterior segment of the eye HPO Gene-Disease Associations 1.0 null optic disc pallor HPO Gene-Disease Associations 1.0 null Amblyopia HuGE Navigator Gene-Phenotype Associations 1.0 null catalytic activity GO Molecular Function Annotations 2015 1.0 null abnormal nervous system electrophysiology HPO Gene-Disease Associations 1.0 null Hearing Loss, Sensorineural HuGE Navigator Gene-Phenotype Associations 1.0 null lipomatous tumor HPO Gene-Disease Associations 1.0 null spontaneous hematomas HPO Gene-Disease Associations 1.0 null SR-786 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -2.05399 nd3 GeneRIF Biological Term Annotations 1.0 null SNCA Hub Proteins Protein-Protein Interactions 1.0 null abnormality of the fundus HPO Gene-Disease Associations 1.0 null Microcephaly DisGeNET Gene-Disease Associations 1.0 null Autism DisGeNET Gene-Disease Associations 1.0 null Respiratory Insufficiency DisGeNET Gene-Phenotype Associations 1.0 null abnormality of adrenal physiology HPO Gene-Disease Associations 1.0 null nadh dehydrogenase (quinone) activity GO Molecular Function Annotations 2015 1.0 null abnormality of the outer ear HPO Gene-Disease Associations 1.0 null muscle GeneRIF Biological Term Annotations 1.0 null WSU-NHL Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.12739 Pulmonary Embolism DisGeNET Gene-Disease Associations 1.0 null Myoclonic Epilepsy DisGeNET Gene-Disease Associations 1.0 null integral component of membrane GO Cellular Component Annotations 2015 1.0 null m10191tc GeneRIF Biological Term Annotations 1.0 null Hyperventilation DisGeNET Gene-Phenotype Associations 1.0 null visual impairment HPO Gene-Disease Associations 1.0 null syndrome GeneRIF Biological Term Annotations 1.0 null aging GeneRIF Biological Term Annotations 1.0 null parkinson GeneRIF Biological Term Annotations 1.0 null codons GeneRIF Biological Term Annotations 1.0 null PA-TU-8902 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.12739 cerebral atrophy HPO Gene-Disease Associations 1.0 null multiple sclerosis GAD Gene-Disease Associations 1.0 null abnormality of divalent inorganic cation homeostasis HPO Gene-Disease Associations 1.0 null morphological abnormality of the gastrointestinal tract HPO Gene-Disease Associations 1.0 null hsa-let-7c-5p MiRTarBase microRNA Targets 1.0 null HCC4011 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.35189 strokelike GeneRIF Biological Term Annotations 1.0 null OVCAR-8 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.05809 abnormality of nervous system morphology HPO Gene-Disease Associations 1.0 null Central Retinal Vessel Vascular Tortuosity DisGeNET Gene-Phenotype Associations 1.0 null leighlike GeneRIF Biological Term Annotations 1.0 null Short Stature, Ctcae DisGeNET Gene-Phenotype Associations 1.0 null Feeding Difficulties In Infancy DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the urinary system physiology HPO Gene-Disease Associations 1.0 null Severe Global Developmental Delay DisGeNET Gene-Phenotype Associations 1.0 null delayed skeletal maturation HPO Gene-Disease Associations 1.0 null catalytic complex GO Cellular Component Annotations 2015 1.0 null nausea and vomiting HPO Gene-Disease Associations 1.0 null Cerebral Ventriculomegaly DisGeNET Gene-Phenotype Associations 1.0 null IM-95M Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 Glaucoma, Open-Angle HuGE Navigator Gene-Phenotype Associations 1.0 null pulmonary hypertension HPO Gene-Disease Associations 1.0 null allele GeneRIF Biological Term Annotations 1.0 null abnormal respiratory system morphology HPO Gene-Disease Associations 1.0 null Memory Impairment DisGeNET Gene-Phenotype Associations 1.0 null Blurred Vision, Ctcae DisGeNET Gene-Phenotype Associations 1.0 null JNJ-38877605 DeepCoverMOA Drug Mechanisms of Action 1.0 0.3 abnormality of immune system physiology HPO Gene-Disease Associations 1.0 null mtnd4 GeneRIF Biological Term Annotations 1.0 null abnormality of the orbital region HPO Gene-Disease Associations 1.0 null Sudden Cardiac Death DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the gingiva HPO Gene-Disease Associations 1.0 null Liver Failure DisGeNET Gene-Disease Associations 1.0 null amino GeneRIF Biological Term Annotations 1.0 null exercise GeneRIF Biological Term Annotations 1.0 null Acute Kidney Injury CTD Gene-Disease Associations 1.0 1.01625 nadh dehydrogenase complex GO Cellular Component Annotations 2015 1.0 null leigh GeneRIF Biological Term Annotations 1.0 null weakness due to upper motor neuron dysfunction HPO Gene-Disease Associations 1.0 null Leigh Disease HuGE Navigator Gene-Phenotype Associations 1.0 null reduced tendon reflexes HPO Gene-Disease Associations 1.0 null abnormality of pancreas physiology HPO Gene-Disease Associations 1.0 null hemiplegia/hemiparesis HPO Gene-Disease Associations 1.0 null M059J Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.04602 abnormality of skeletal physiology HPO Gene-Disease Associations 1.0 null memory impairment HPO Gene-Disease Associations 1.0 null hypertrophic GeneRIF Biological Term Annotations 1.0 null NSC 23766 DeepCoverMOA Drug Mechanisms of Action -1.0 -0.32 embryos GeneRIF Biological Term Annotations 1.0 null neversmoker GeneRIF Biological Term Annotations 1.0 null abnormality of the integument HPO Gene-Disease Associations 1.0 null ZR-75-30 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 organelle part GO Cellular Component Annotations 2015 1.0 null congenital contracture HPO Gene-Disease Associations 1.0 null SB 525334 DeepCoverMOA Drug Mechanisms of Action -1.0 -0.71 changes GeneRIF Biological Term Annotations 1.0 null Guanfacine DeepCoverMOA Drug Mechanisms of Action -1.0 -0.8 Idiopathic Pulmonary Arterial Hypertension DisGeNET Gene-Disease Associations 1.0 null Bulbar Signs DisGeNET Gene-Phenotype Associations 1.0 null constipation HPO Gene-Disease Associations 1.0 null Insulin Resistance HuGE Navigator Gene-Phenotype Associations 1.0 null boy GeneRIF Biological Term Annotations 1.0 null CZC-25146 DeepCoverMOA Drug Mechanisms of Action 1.0 0.5 Leigh Disease DisGeNET Gene-Disease Associations 1.0 null PMC5777890__F7 PFOCR Pathway Figure Associations 2023 1.0 null hsa-miR-1180-3p MiRTarBase microRNA Targets 1.0 null melas GeneRIF Biological Term Annotations 1.0 null intracellular organelle part GO Cellular Component Annotations 2015 1.0 null present GeneRIF Biological Term Annotations 1.0 null point GeneRIF Biological Term Annotations 1.0 null Generalized Myoclonic Seizures DisGeNET Gene-Disease Associations 1.0 null gastrointestinal obstruction HPO Gene-Disease Associations 1.0 null ubiquinone biosynthesis KEGG Pathways 1.0 null thyroiditis HPO Gene-Disease Associations 1.0 null Melas Syndrome DisGeNET Gene-Disease Associations 1.0 null abnormal retinal pigmentation HPO Gene-Disease Associations 1.0 null intrinsic component of membrane GO Cellular Component Annotations 2015 1.0 null hypertelorism HPO Gene-Disease Associations 1.0 null Psychotic Episodes DisGeNET Gene-Disease Associations 1.0 null abnormality of the endocrine system HPO Gene-Disease Associations 1.0 null large central visual field defect HPO Gene-Disease Associations 1.0 null hsa-miR-296-3p MiRTarBase microRNA Targets 1.0 null Ragged-Red Muscle Fibers DisGeNET Gene-Phenotype Associations 1.0 null describes GeneRIF Biological Term Annotations 1.0 null defect GeneRIF Biological Term Annotations 1.0 null Parkinson Disease DisGeNET Gene-Disease Associations 1.0 null Skeletal Muscle Atrophy DisGeNET Gene-Phenotype Associations 1.0 null Tonic - Clonic Seizures DisGeNET Gene-Disease Associations 1.0 null Fever DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the genital system HPO Gene-Disease Associations 1.0 null Lorcaserin DeepCoverMOA Drug Mechanisms of Action 1.0 0.59 Hypertrophic Cardiomyopathy DisGeNET Gene-Disease Associations 1.0 null Diabetes DisGeNET Gene-Disease Associations 1.0 null single-organism cellular process GO Biological Process Annotations 2015 1.0 null abnormality of the abdominal organs HPO Gene-Disease Associations 1.0 null Schizophrenia HuGE Navigator Gene-Phenotype Associations 1.0 null small GeneRIF Biological Term Annotations 1.0 null Parkinson Disease HuGE Navigator Gene-Phenotype Associations 1.0 null oxidative phosphorylation KEGG Pathways 1.0 null Increased Csf Lactate DisGeNET Gene-Phenotype Associations 1.0 null all HPO Gene-Disease Associations 1.0 null Minocycline DeepCoverMOA Drug Mechanisms of Action -1.0 -0.42 Ventricular Preexcitation DisGeNET Gene-Disease Associations 1.0 null Glomerulopathy Assessment DisGeNET Gene-Phenotype Associations 1.0 null Lactic Aciduria DisGeNET Gene-Phenotype Associations 1.0 null oxidoreductase activity GO Molecular Function Annotations 2015 1.0 null Muscle Hypotonia DisGeNET Gene-Phenotype Associations 1.0 null lung GeneRIF Biological Term Annotations 1.0 null abnormality of hindbrain morphology HPO Gene-Disease Associations 1.0 null abnormality of the skeletal system HPO Gene-Disease Associations 1.0 null involuntary movements HPO Gene-Disease Associations 1.0 null Orbital Separation Excessive DisGeNET Gene-Phenotype Associations 1.0 null High Altitude Pulmonary Edema DisGeNET Gene-Disease Associations 1.0 null Alcoholism HuGE Navigator Gene-Phenotype Associations 1.0 null abnormality of oral mucosa HPO Gene-Disease Associations 1.0 null Blepharoptosis DisGeNET Gene-Disease Associations 1.0 null HCC1576 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.849775 mitochondrial electron transport, nadh to ubiquinone GO Biological Process Annotations 2015 1.0 null Generalized Hirsutism DisGeNET Gene-Phenotype Associations 1.0 null macromolecular complex GO Cellular Component Annotations 2015 1.0 null consumption GeneRIF Biological Term Annotations 1.0 null G84 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.862816 Optic Atrophy, Hereditary, Leber HuGE Navigator Gene-Phenotype Associations 1.0 null Overlap Syndrome DisGeNET Gene-Disease Associations 1.0 null Mitochondrial Encephalopathy, Lactic Acidosis And Stroke-Like Episodes (Melas Syndrome) DisGeNET Gene-Disease Associations 1.0 null muscular hypotonia HPO Gene-Disease Associations 1.0 null suspected GeneRIF Biological Term Annotations 1.0 null congestive heart failure HPO Gene-Disease Associations 1.0 null organelle membrane GO Cellular Component Annotations 2015 1.0 null mucosa GeneRIF Biological Term Annotations 1.0 null mutational GeneRIF Biological Term Annotations 1.0 null abnormality of cardiovascular system physiology HPO Gene-Disease Associations 1.0 null Abdominal Pain DisGeNET Gene-Phenotype Associations 1.0 null parkinson's disease GAD Gene-Disease Associations 1.0 null pathogenic GeneRIF Biological Term Annotations 1.0 null Abnormal Speech Prosody DisGeNET Gene-Phenotype Associations 1.0 null adrenal insufficiency HPO Gene-Disease Associations 1.0 null Dementia DisGeNET Gene-Disease Associations 1.0 null attention deficit hyperactivity disorder HPO Gene-Disease Associations 1.0 null Aphasia DisGeNET Gene-Disease Associations 1.0 null mask-like facies HPO Gene-Disease Associations 1.0 null abnormality of cation homeostasis HPO Gene-Disease Associations 1.0 null Adenocarcinoma DisGeNET Gene-Disease Associations 1.0 null hearing impairment HPO Gene-Disease Associations 1.0 null abnormal axial skeleton morphology HPO Gene-Disease Associations 1.0 null hsa-miR-320a MiRTarBase microRNA Targets 1.0 null atrophy/degeneration affecting the central nervous system HPO Gene-Disease Associations 1.0 null pathological GeneRIF Biological Term Annotations 1.0 null Hypothyroidism DisGeNET Gene-Disease Associations 1.0 null Ophthalmoparesis DisGeNET Gene-Phenotype Associations 1.0 null atp GeneRIF Biological Term Annotations 1.0 null maternally GeneRIF Biological Term Annotations 1.0 null Arthrogryposis DisGeNET Gene-Disease Associations 1.0 null abnormality of ion homeostasis HPO Gene-Disease Associations 1.0 null resulted GeneRIF Biological Term Annotations 1.0 null ectopic calcification HPO Gene-Disease Associations 1.0 null abnormality of the anterior pituitary HPO Gene-Disease Associations 1.0 null hsa-let-7e-5p MiRTarBase microRNA Targets 1.0 null type i diabetes mellitus HPO Gene-Disease Associations 1.0 null neoplasm by anatomical site HPO Gene-Disease Associations 1.0 null common GeneRIF Biological Term Annotations 1.0 null platelets GeneRIF Biological Term Annotations 1.0 null type ii diabetes mellitus HPO Gene-Disease Associations 1.0 null abnormality of central motor function HPO Gene-Disease Associations 1.0 null segregate GeneRIF Biological Term Annotations 1.0 null cerebral ischemia HPO Gene-Disease Associations 1.0 null abnormality of thyroid physiology HPO Gene-Disease Associations 1.0 null abnormality of the pancreas HPO Gene-Disease Associations 1.0 null preferential GeneRIF Biological Term Annotations 1.0 null Cardiac Arrhythmia DisGeNET Gene-Phenotype Associations 1.0 null Gingival Overgrowth DisGeNET Gene-Phenotype Associations 1.0 null Ibutamoren DeepCoverMOA Drug Mechanisms of Action -1.0 -0.35 upper motor neuron dysfunction HPO Gene-Disease Associations 1.0 null OAW42 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 SW 948 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 epilepsy GeneRIF Biological Term Annotations 1.0 null clinical GeneRIF Biological Term Annotations 1.0 null Creatine Phosphokinase Serum Increased DisGeNET Gene-Phenotype Associations 1.0 null WZ811 DeepCoverMOA Drug Mechanisms of Action -1.0 -0.55 Dissection Of Aorta DisGeNET Gene-Disease Associations 1.0 null pancreatitis HPO Gene-Disease Associations 1.0 null Glycogen Storage Disease DisGeNET Gene-Disease Associations 1.0 null abnormality of the optic nerve HPO Gene-Disease Associations 1.0 null Visual Impairment DisGeNET Gene-Phenotype Associations 1.0 null neurodevelopmental abnormality HPO Gene-Disease Associations 1.0 null dur GeneRIF Biological Term Annotations 1.0 null hearing abnormality HPO Gene-Disease Associations 1.0 null glomerulopathy HPO Gene-Disease Associations 1.0 null Wolff-Parkinson-White Syndrome HuGE Navigator Gene-Phenotype Associations 1.0 null abnormality of skin pigmentation HPO Gene-Disease Associations 1.0 null gingival overgrowth HPO Gene-Disease Associations 1.0 null abnormality of peripheral nervous system electrophysiology HPO Gene-Disease Associations 1.0 null sudden cardiac death HPO Gene-Disease Associations 1.0 null Hypothermia, Natural DisGeNET Gene-Phenotype Associations 1.0 null showing GeneRIF Biological Term Annotations 1.0 null multiple lipomas HPO Gene-Disease Associations 1.0 null abnormality of the oral cavity HPO Gene-Disease Associations 1.0 null three GeneRIF Biological Term Annotations 1.0 null pulmonary embolism HPO Gene-Disease Associations 1.0 null Dysarthria DisGeNET Gene-Disease Associations 1.0 null COLO 849 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 Variable Expressivity DisGeNET Gene-Phenotype Associations 1.0 null Impaired Cognition DisGeNET Gene-Disease Associations 1.0 null intestinal obstruction HPO Gene-Disease Associations 1.0 null Generalized Glycogen Storage Disease Of Infants DisGeNET Gene-Disease Associations 1.0 null pedigree GeneRIF Biological Term Annotations 1.0 null neurological speech impairment HPO Gene-Disease Associations 1.0 null Leigh Syndrome Due To Mitochondrial Complex I Deficiency DisGeNET Gene-Disease Associations 1.0 null Retinitis Pigmentosa DisGeNET Gene-Disease Associations 1.0 null abnormality of the cerebrum HPO Gene-Disease Associations 1.0 null genetic diseases, inborn; hearing impairment; hearing loss GAD Gene-Disease Associations 1.0 null dexamethasone_rattus norvegicus_gpl85_gse6216 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null characteristic GeneRIF Biological Term Annotations 1.0 null hypercalciuria HPO Gene-Disease Associations 1.0 null respiratory chain complex i GO Cellular Component Annotations 2015 1.0 null Progressive Sensorineural Hearing Impairment DisGeNET Gene-Disease Associations 1.0 null epidermal thickening HPO Gene-Disease Associations 1.0 null secondary GeneRIF Biological Term Annotations 1.0 null dysfunction GeneRIF Biological Term Annotations 1.0 null A 438079 DeepCoverMOA Drug Mechanisms of Action 1.0 0.27 HEY Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.46316 controls GeneRIF Biological Term Annotations 1.0 null abnormality of skull size HPO Gene-Disease Associations 1.0 null abnormality of the pinna HPO Gene-Disease Associations 1.0 null complete GeneRIF Biological Term Annotations 1.0 null macular degeneration GAD Gene-Disease Associations 1.0 null Congestive Heart Failure DisGeNET Gene-Disease Associations 1.0 null Lasmiditan DeepCoverMOA Drug Mechanisms of Action -1.0 -0.25 abnormality of the kidney HPO Gene-Disease Associations 1.0 null low GeneRIF Biological Term Annotations 1.0 null synrome GeneRIF Biological Term Annotations 1.0 null hyperactivity HPO Gene-Disease Associations 1.0 null feeding difficulties in infancy HPO Gene-Disease Associations 1.0 null ABC-1 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 atypical GeneRIF Biological Term Annotations 1.0 null inheritance GeneRIF Biological Term Annotations 1.0 null Developmental Regression DisGeNET Gene-Disease Associations 1.0 null breast cancer GAD Gene-Disease Associations 1.0 null abnormality of the pituitary gland HPO Gene-Disease Associations 1.0 null oxidation-reduction process GO Biological Process Annotations 2015 1.0 null oxidoreductase activity, acting on nad(p)h, quinone or similar compound as acceptor GO Molecular Function Annotations 2015 1.0 null MX-1 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 hsa-miR-186-5p MiRTarBase microRNA Targets 1.0 null Eniporide DeepCoverMOA Drug Mechanisms of Action -1.0 -0.28 biological_process GO Biological Process Annotations 2015 1.0 null abnormality of metabolism/homeostasis HPO Gene-Disease Associations 1.0 null MELAS Syndrome HuGE Navigator Gene-Phenotype Associations 1.0 null alzheimer's disease GAD Gene-Disease Associations 1.0 null Cerebral Ischemia DisGeNET Gene-Disease Associations 1.0 null abnormality of the upper urinary tract HPO Gene-Disease Associations 1.0 null diabetes mellitus HPO Gene-Disease Associations 1.0 null visual field defect HPO Gene-Disease Associations 1.0 null CI-1 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.82847 Retinal Telangiectasia DisGeNET Gene-Disease Associations 1.0 null Goiter DisGeNET Gene-Phenotype Associations 1.0 null methylprednisolone_rattus norvegicus_gpl85_gds965 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null HM7 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.89415 abnormality of nervous system physiology HPO Gene-Disease Associations 1.0 null abnormality of brain morphology HPO Gene-Disease Associations 1.0 null MK-6892 DeepCoverMOA Drug Mechanisms of Action -1.0 -0.29 Drug-Induced Liver Injury CTD Gene-Disease Associations 1.0 1.267 italian GeneRIF Biological Term Annotations 1.0 null multiple GeneRIF Biological Term Annotations 1.0 null abnormality of the respiratory system HPO Gene-Disease Associations 1.0 null MKN-1 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.36193 muscle weakness HPO Gene-Disease Associations 1.0 null Episodic Vomiting DisGeNET Gene-Phenotype Associations 1.0 null abnormality of mitochondrial metabolism HPO Gene-Disease Associations 1.0 null MKN-74 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.75136 functional abnormality of the gastrointestinal tract HPO Gene-Disease Associations 1.0 null mitochondrial inheritance HPO Gene-Disease Associations 1.0 null 928 MEL Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.916601 JHH-4 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.28606 abnormal eye physiology HPO Gene-Disease Associations 1.0 null Cerebral Cortical Atrophy DisGeNET Gene-Disease Associations 1.0 null atrophy GeneRIF Biological Term Annotations 1.0 null Slow Decrease In Visual Acuity DisGeNET Gene-Phenotype Associations 1.0 null Breast Fibrocystic Disease DisGeNET Gene-Disease Associations 1.0 null thickened skin HPO Gene-Disease Associations 1.0 null MDA-MB-175-VII Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 conclude GeneRIF Biological Term Annotations 1.0 null intolerance GeneRIF Biological Term Annotations 1.0 null abnormal joint morphology HPO Gene-Disease Associations 1.0 null absence GeneRIF Biological Term Annotations 1.0 null accounting GeneRIF Biological Term Annotations 1.0 null hsa-let-7f-5p MiRTarBase microRNA Targets 1.0 null Low Plasma Citrulline DisGeNET Gene-Phenotype Associations 1.0 null PF-431396 DeepCoverMOA Drug Mechanisms of Action 1.0 0.97 MOR Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 line GeneRIF Biological Term Annotations 1.0 null abnormality of the cerebral ventricles HPO Gene-Disease Associations 1.0 null abnormality of central nervous system electrophysiology HPO Gene-Disease Associations 1.0 null SYK_druginhibition_285_GSE43510 GEO Signatures of Differentially Expressed Genes for Kinase Perturbations 1.0 1.08816 had GeneRIF Biological Term Annotations 1.0 null cardiac arrest HPO Gene-Disease Associations 1.0 null abnormality of the systemic arterial tree HPO Gene-Disease Associations 1.0 null proteinuria HPO Gene-Disease Associations 1.0 null BFTC-905 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.890749 abnormality of cardiac morphology HPO Gene-Disease Associations 1.0 null abnormality of blood and blood-forming tissues HPO Gene-Disease Associations 1.0 null likely GeneRIF Biological Term Annotations 1.0 null abnormality of thyroid morphology HPO Gene-Disease Associations 1.0 null GSK429286A DeepCoverMOA Drug Mechanisms of Action -1.0 -0.28 Post-Traumatic Stress Disorder DisGeNET Gene-Disease Associations 1.0 null subcutaneous hemorrhage HPO Gene-Disease Associations 1.0 null amaurosis fugax HPO Gene-Disease Associations 1.0 null Amyotrophic Lateral Sclerosis DisGeNET Gene-Disease Associations 1.0 null abnormal eye morphology HPO Gene-Disease Associations 1.0 null maternal GeneRIF Biological Term Annotations 1.0 null Hyporeflexia DisGeNET Gene-Phenotype Associations 1.0 null transition GeneRIF Biological Term Annotations 1.0 null abnormality of the nervous system HPO Gene-Disease Associations 1.0 null Polyneuropathy DisGeNET Gene-Disease Associations 1.0 null Mask-Like Facies DisGeNET Gene-Phenotype Associations 1.0 null Ascomycin DeepCoverMOA Drug Mechanisms of Action -1.0 -0.91 parkinsons GeneRIF Biological Term Annotations 1.0 null Hallucinations DisGeNET Gene-Disease Associations 1.0 null Blurred Vision DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the inner ear HPO Gene-Disease Associations 1.0 null GTL-16 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -2.31075 Hyperreflexia DisGeNET Gene-Phenotype Associations 1.0 null load GeneRIF Biological Term Annotations 1.0 null Rotigotine DeepCoverMOA Drug Mechanisms of Action -1.0 -0.38 abnormality of coordination HPO Gene-Disease Associations 1.0 null Pulmonary Arterial Hypertension DisGeNET Gene-Disease Associations 1.0 null L-165041 DeepCoverMOA Drug Mechanisms of Action -1.0 -0.42 renal insufficiency HPO Gene-Disease Associations 1.0 null respiratory insufficiency HPO Gene-Disease Associations 1.0 null arterial stenosis HPO Gene-Disease Associations 1.0 null Hypercalciuria DisGeNET Gene-Phenotype Associations 1.0 null SR 11237 DeepCoverMOA Drug Mechanisms of Action 1.0 0.32 DLD-1 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 oxidoreductase complex GO Cellular Component Annotations 2015 1.0 null conserved GeneRIF Biological Term Annotations 1.0 null Mitochondrial Cardiomyopathy DisGeNET Gene-Disease Associations 1.0 null Ptosis DisGeNET Gene-Disease Associations 1.0 null Esophageal Carcinoma DisGeNET Gene-Disease Associations 1.0 null Clonus DisGeNET Gene-Phenotype Associations 1.0 null susceptibility GeneRIF Biological Term Annotations 1.0 null Infantile Muscular Hypotonia DisGeNET Gene-Phenotype Associations 1.0 null Hyper-Beta-Alaninemia DisGeNET Gene-Phenotype Associations 1.0 null abnormality of connective tissue HPO Gene-Disease Associations 1.0 null NADH:quinone oxidoreductase/Mrp antiporter, membrane subunit InterPro Predicted Protein Domain Annotations 1.0 null describe GeneRIF Biological Term Annotations 1.0 null West Syndrome DisGeNET Gene-Disease Associations 1.0 null colorectal GeneRIF Biological Term Annotations 1.0 null abnormality of the ocular region HPO Gene-Disease Associations 1.0 null Tumor Progression DisGeNET Gene-Phenotype Associations 1.0 null lhon GeneRIF Biological Term Annotations 1.0 null accumulate GeneRIF Biological Term Annotations 1.0 null tibet GeneRIF Biological Term Annotations 1.0 null Anterior Hypopituitarism DisGeNET Gene-Disease Associations 1.0 null small molecule metabolic process GO Biological Process Annotations 2015 1.0 null reported GeneRIF Biological Term Annotations 1.0 null vibrio GeneRIF Biological Term Annotations 1.0 null abnormality of muscle physiology HPO Gene-Disease Associations 1.0 null severe GeneRIF Biological Term Annotations 1.0 null NCI-H2172 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 there GeneRIF Biological Term Annotations 1.0 null LCLC-103H Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.13884 Nystagmus DisGeNET Gene-Disease Associations 1.0 null 537 MEL Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -0.862816 hypopigmented skin patches HPO Gene-Disease Associations 1.0 null abnormality of the macula HPO Gene-Disease Associations 1.0 null microcephaly HPO Gene-Disease Associations 1.0 null hotspots GeneRIF Biological Term Annotations 1.0 null cerebral calcification HPO Gene-Disease Associations 1.0 null hallucinations HPO Gene-Disease Associations 1.0 null Nicotinamide Adenine Dinucleotide Coenzyme Q Reductase Deficiency DisGeNET Gene-Disease Associations 1.0 null SCC-9 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.52298 Anorexia DisGeNET Gene-Disease Associations 1.0 null genetic GeneRIF Biological Term Annotations 1.0 null sclerosis GeneRIF Biological Term Annotations 1.0 null Growth Abnormality DisGeNET Gene-Phenotype Associations 1.0 null heteroplasmic GeneRIF Biological Term Annotations 1.0 null intracellular part GO Cellular Component Annotations 2015 1.0 null Aplasia/Hypoplasia Of The Cerebellum DisGeNET Gene-Phenotype Associations 1.0 null peripheral neuropathy HPO Gene-Disease Associations 1.0 null Failure To Thrive DisGeNET Gene-Disease Associations 1.0 null Biventricular Hypertrophy DisGeNET Gene-Disease Associations 1.0 null abnormality of skeletal morphology HPO Gene-Disease Associations 1.0 null LP-533401 DeepCoverMOA Drug Mechanisms of Action -1.0 -0.36 A 967079 DeepCoverMOA Drug Mechanisms of Action 1.0 0.29 Thyroiditis DisGeNET Gene-Disease Associations 1.0 null PANC 02.03 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles -1.0 -1.23571 NCI-H1568 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 1.21535 abnormality of the hair HPO Gene-Disease Associations 1.0 null Muscle Weakness DisGeNET Gene-Phenotype Associations 1.0 null Hemianopsia DisGeNET Gene-Disease Associations 1.0 null importance GeneRIF Biological Term Annotations 1.0 null cortex GeneRIF Biological Term Annotations 1.0 null characterization GeneRIF Biological Term Annotations 1.0 null Paresthesia DisGeNET Gene-Phenotype Associations 1.0 null genome GeneRIF Biological Term Annotations 1.0 null mitochondrial respiratory chain complex i GO Cellular Component Annotations 2015 1.0 null Electron Transport Chain(Mus musculus) WikiPathways Pathways 2014 1.0 null abnormality of the teeth HPO Gene-Disease Associations 1.0 null PP2 DeepCoverMOA Drug Mechanisms of Action -1.0 -0.71 FR 180204 DeepCoverMOA Drug Mechanisms of Action 1.0 0.83 optic atrophy HPO Gene-Disease Associations 1.0 null abnormality of movement HPO Gene-Disease Associations 1.0 null MOLM-16 Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles 1.0 0.957857 IWR-1 DeepCoverMOA Drug Mechanisms of Action 1.0 0.32 mutant GeneRIF Biological Term Annotations 1.0 null abnormality of the parathyroid physiology HPO Gene-Disease Associations 1.0 null Pimavanserin DeepCoverMOA Drug Mechanisms of Action -1.0 -0.43 Static Tremor DisGeNET Gene-Phenotype Associations 1.0 null cognitive ability GAD Gene-Disease Associations 1.0 null PF-514273 DeepCoverMOA Drug Mechanisms of Action -1.0 -0.41 hypoparathyroidism HPO Gene-Disease Associations 1.0 null