LRpath

Pathway Analysis using Logistic Regression
Browse Concepts
Concept Name Gene List Download
Adrenoleukodystrophy hsa mmu rno
Agammaglobulinemia hsa mmu rno
AIDS hsa mmu rno
Alcohol dependence hsa mmu rno
Alopecia hsa mmu rno
Alzheimer disease hsa mmu rno
Amelogenesis imperfecta hsa mmu rno
Amyotrophic lateral sclerosis hsa mmu rno
Anemia hsa mmu rno
Aneurysm hsa mmu rno
Arrhythmogenic right ventricular dysplasia hsa mmu rno
Arthrogryposis hsa mmu rno
Asthma hsa mmu rno
Ataxia hsa mmu rno
Atrial fibrillation hsa mmu rno
Atrial septal defect hsa mmu rno
Attention deficit-hyperactivity disorder hsa mmu rno
Autism hsa mmu rno
Autoimmune disease hsa mmu rno
Bardet-Biedl syndrome hsa mmu rno
Bare lymphocyte syndrome hsa mmu rno
Bartter syndrome hsa mmu rno
Basal cell carcinoma hsa mmu rno
Body mass index QTL hsa mmu rno
Brachydactyly hsa mmu rno
Breast cancer hsa mmu rno
Brugada syndrome hsa mmu rno
Cardiomyopathy hsa mmu rno
Cataract hsa mmu rno
Celiac disease hsa mmu rno
Ceroid lipofuscinosis, neuronal hsa mmu rno
Charcot-Marie-Tooth disease hsa mmu rno
Cholestasis hsa mmu rno
Ciliary dyskinesia hsa mmu rno
Cleft palate hsa mmu rno
Coenzyme Q10 deficiency hsa mmu rno
Colon cancer hsa mmu rno
Colorectal cancer hsa mmu rno
Combined oxidative phosphorylation deficiency hsa mmu rno
Cone-rod dystrophy hsa mmu rno
Congenital disorder of glycosylation hsa mmu rno
Convulsions hsa mmu rno
Corneal dystrophy hsa mmu rno
Coronary artery disease hsa mmu rno
Coronary heart disease hsa mmu rno
Cutis laxa hsa mmu rno
Deafness hsa mmu rno
Dermatitis, atopic hsa mmu rno
Diabetes mellitus, insulin-dependent hsa mmu rno
Diabetes mellitus, noninsulin-dependent hsa mmu rno
Diamond-Blackfan anemia hsa mmu rno
Dyskeratosis hsa mmu rno
Dyslexia hsa mmu rno
Dystonia hsa mmu rno
Ectodermal dysplasia hsa mmu rno
Ehlers-Danlos syndrome hsa mmu rno
Encephalopathy hsa mmu rno
Epidermolysis bullosa hsa mmu rno
Epilepsy hsa mmu rno
Epileptic encephalopathy hsa mmu rno
Esophageal cancer hsa mmu rno
Fanconi anemia hsa mmu rno
Fibromatosis hsa mmu rno
Fibrosis of extraocular muscles, congenital hsa mmu rno
Glaucoma hsa mmu rno
Glucocorticoid deficiency hsa mmu rno
Glutaricaciduria hsa mmu rno
Glycogen storage disease hsa mmu rno
Hemangioma hsa mmu rno
Hemolytic anemia hsa mmu rno
Hemolytic uremic syndrome hsa mmu rno
Hemophagocytic lymphohistiocytosis hsa mmu rno
Hermansky-Pudlak syndrome hsa mmu rno
High density lipoprotien cholesterol level QTL hsa mmu rno
HIV infection hsa mmu rno
Holoprosencephaly hsa mmu rno
Hypercholesterolemia hsa mmu rno
Hypertension hsa mmu rno
Hypogonadotropic hypogonadism hsa mmu rno
Hypomagnesemia hsa mmu rno
Hypotrichosis hsa mmu rno
Ichthyosis hsa mmu rno
Immunodeficiency hsa mmu rno
Inflammatory bowel disease hsa mmu rno
Joubert syndrome hsa mmu rno
Leber congenital amaurosis hsa mmu rno
Leigh syndrome hsa mmu rno
Leukemia hsa mmu rno
Leukodystrophy hsa mmu rno
Leukoencephalopathy hsa mmu rno
Lipodystrophy hsa mmu rno
Long QT syndrome hsa mmu rno
Lung cancer hsa mmu rno
Macular degeneration, age-related hsa mmu rno
Macular dystrophy hsa mmu rno
Malaria hsa mmu rno
Malignant hyperthermia susceptibility hsa mmu rno
Melanoma hsa mmu rno
Mental retardation hsa mmu rno
Methylmalonic aciduria hsa mmu rno
Microcephaly hsa mmu rno
Microphthalmia hsa mmu rno
Migraine hsa mmu rno
Mitochondrial complex I deficiency hsa mmu rno
Mitochondrial DNA depletion syndrome hsa mmu rno
Mucopolysaccharidosis hsa mmu rno
Muscular dystrophy hsa mmu rno
Myocardial infarction hsa mmu rno
Myopathy hsa mmu rno
Myopia hsa mmu rno
Nemaline myopathy hsa mmu rno
Neuroblastoma hsa mmu rno
Neuropathy hsa mmu rno
Night blindness hsa mmu rno
Nystagmus hsa mmu rno
Obesity hsa mmu rno
Optic atrophy hsa mmu rno
Orofacial cleft hsa mmu rno
Osteopetrosis hsa mmu rno
Otosclerosis hsa mmu rno
Ovarian cancer hsa mmu rno
Parkinson disease hsa mmu rno
Pontocerebellar hypoplasia hsa mmu rno
Preeclampsia hsa mmu rno
Prostate cancer hsa mmu rno
Psoriasis hsa mmu rno
Refsum disease hsa mmu rno
Renal cell carcinoma hsa mmu rno
Retinitis pigmentosa hsa mmu rno
Rheumatoid arthritis hsa mmu rno
Schizophrenia hsa mmu rno
Skin/hair/eye pigmentation hsa mmu rno
Spastic paraplegia hsa mmu rno
Spinal muscular atrophy hsa mmu rno
Spinocerebellar ataxia hsa mmu rno
Split hand/foot malformation hsa mmu rno
Stature QTL hsa mmu rno
Systemic lupus erythematosus hsa mmu rno
Thrombophilia hsa mmu rno
Thyroid carcinoma hsa mmu rno
Xeroderma pigmentosum hsa mmu rno
Zellweger syndrome hsa mmu rno



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Grant # R01 LM008106 ("Representing and Acquiring Knowledge of Genome
Regulation") and the National Center for Integrative Biomedical
Informatics (NCIBI), NIH Grant # U54 DA021519 01A1
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