* We recommend a score >= 0.08 for meaningful Gene-Disease associations
GeneID | Gene_Symbol | DisGeNet_diseaseID | Disease_name | DisGeNet score | DisGeNet_sourceDB |
7415 | VCP | C1833662 | INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA | 0.688791257094819 | BEFREE;CTD_human;MGD;ORPHANET;UNIPROT |
7415 | VCP | C0002736 | Amyotrophic Lateral Sclerosis | 0.412846646323386 | BEFREE;GAD;HPO;ORPHANET |
7415 | VCP | C4225244 | CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y | 0.4 | ORPHANET;UNIPROT |
7415 | VCP | C0026848 | Myopathy | 0.228774535455789 | BEFREE;HPO;LHGDN |
7415 | VCP | C0338451 | Frontotemporal dementia | 0.218406694542278 | BEFREE;HPO |
7415 | VCP | C0151786 | Muscle Weakness | 0.204106546385879 | BEFREE;HPO;LHGDN |
7415 | VCP | C0524851 | Neurodegenerative Disorders | 0.201923087489492 | BEFREE;HPO |
7415 | VCP | C0338462 | Semantic Dementia | 0.200274726784213 | BEFREE;ORPHANET |
7415 | VCP | C0001807 | Aggressive behavior | 0.2 | HPO |
7415 | VCP | C0002018 | Alexia | 0.2 | HPO |
7415 | VCP | C0003467 | Anxiety | 0.2 | HPO |
7415 | VCP | C0003635 | Apraxias | 0.2 | HPO |
7415 | VCP | C0003862 | Arthralgia | 0.2 | HPO |
7415 | VCP | C0004604 | Back Pain | 0.2 | HPO |
7415 | VCP | C0011581 | Depressive disorder | 0.2 | HPO |
7415 | VCP | C0013362 | Dysarthria | 0.2 | HPO |
7415 | VCP | C0013404 | Dyspnea | 0.2 | HPO |
7415 | VCP | C0013421 | Dystonia | 0.2 | HPO |
7415 | VCP | C0013528 | Echolalia | 0.2 | HPO |
7415 | VCP | C0015644 | Muscular fasciculation | 0.2 | HPO |
7415 | VCP | C0015672 | Fatigue | 0.2 | HPO |
7415 | VCP | C0026821 | Muscle Cramp | 0.2 | HPO |
7415 | VCP | C0026838 | Muscle Spasticity | 0.2 | HPO |
7415 | VCP | C0027746 | Nerve Degeneration | 0.2 | HPO |
7415 | VCP | C0030193 | Pain | 0.2 | HPO |
7415 | VCP | C0034935 | Babinski Reflex | 0.2 | HPO |
7415 | VCP | C0037772 | Spastic Paraplegia | 0.2 | HPO |
7415 | VCP | C0038271 | Stereotyped Behavior | 0.2 | HPO |
7415 | VCP | C0038273 | Stereotypic Movement Disorder | 0.2 | HPO |
7415 | VCP | C0038325 | Stevens-Johnson Syndrome | 0.2 | CTD_human |
7415 | VCP | C0043352 | Xerostomia | 0.2 | HPO |
7415 | VCP | C0085633 | Mood swings | 0.2 | HPO |
7415 | VCP | C0151576 | Elevated creatine kinase | 0.2 | HPO |
7415 | VCP | C0221629 | Proximal muscle weakness | 0.2 | HPO |
7415 | VCP | C0231687 | Spastic gait | 0.2 | HPO |
7415 | VCP | C0233794 | Memory impairment | 0.2 | HPO |
7415 | VCP | C0234144 | Dysgraphia | 0.2 | HPO |
7415 | VCP | C0234958 | muscle degeneration | 0.2 | HPO |
7415 | VCP | C0239067 | Difficulty walking up stairs | 0.2 | HPO |
7415 | VCP | C0239548 | Fasciculation, Tongue | 0.2 | HPO |
7415 | VCP | C0240679 | Pelvic girdle muscle atrophy | 0.2 | HPO |
7415 | VCP | C0240735 | Personality change | 0.2 | HPO |
7415 | VCP | C0240953 | Winged scapula | 0.2 | HPO |
7415 | VCP | C0241005 | Creatine phosphokinase serum increased | 0.2 | HPO |
7415 | VCP | C0270948 | Neurogenic Muscular Atrophy | 0.2 | HPO |
7415 | VCP | C0424290 | Compulsive hoarding | 0.2 | HPO |
7415 | VCP | C0424296 | Social disinhibition | 0.2 | HPO |
7415 | VCP | C0424323 | Physical aggression | 0.2 | HPO |
7415 | VCP | C0427063 | Shoulder girdle weakness | 0.2 | HPO |
7415 | VCP | C0427064 | Pelvic girdle weakness | 0.2 | HPO |
7415 | VCP | C0427065 | Distal muscle weakness | 0.2 | HPO |
7415 | VCP | C0476254 | Dyslexia | 0.2 | HPO |
7415 | VCP | C0522224 | Paralysed | 0.2 | HPO |
7415 | VCP | C0541794 | Skeletal muscle atrophy | 0.2 | HPO |
7415 | VCP | C0542223 | Loss of speech | 0.2 | HPO |
7415 | VCP | C0542476 | Forgetful | 0.2 | HPO |
7415 | VCP | C0558845 | Reflex, Ankle, Absent | 0.2 | HPO |
7415 | VCP | C0575081 | Gait abnormality | 0.2 | HPO |
7415 | VCP | C0587246 | Muscle weakness of limb | 0.2 | HPO |
7415 | VCP | C0728829 | Congenital pes cavus | 0.2 | HPO |
7415 | VCP | C0746674 | Generalized muscle weakness | 0.2 | HPO |
7415 | VCP | C0748691 | Shoulder weakness | 0.2 | HPO |
7415 | VCP | C0750857 | Alkaline phosphatase serum increased | 0.2 | HPO |
7415 | VCP | C0751295 | Memory Loss | 0.2 | HPO |
7415 | VCP | C0751706 | Primary Progressive Nonfluent Aphasia | 0.2 | ORPHANET |
7415 | VCP | C0948163 | Leukoaraiosis | 0.2 | HPO |
7415 | VCP | C0973461 | Dysphasia | 0.2 | HPO |
7415 | VCP | C1136179 | Hammer Toe | 0.2 | HPO |
7415 | VCP | C1145670 | Respiratory Failure | 0.2 | HPO |
7415 | VCP | C1184923 | Lumbar lordosis | 0.2 | HPO |
7415 | VCP | C1411876 | Developmental arithmetic disorder | 0.2 | HPO |
7415 | VCP | C1457883 | Aggressive reaction | 0.2 | HPO |
7415 | VCP | C1833667 | Increased serum bone-specific alkaline phosphatase | 0.2 | HPO |
7415 | VCP | C1836150 | Gait imbalance | 0.2 | HPO |
7415 | VCP | C1836696 | Lower limb hyperreflexia | 0.2 | HPO |
7415 | VCP | C1836940 | Excess nuchal skin | 0.2 | HPO |
7415 | VCP | C1838320 | Hyperorality | 0.2 | HPO |
7415 | VCP | C1838869 | Proximal neurogenic muscle weakness | 0.2 | HPO |
7415 | VCP | C1843479 | Neurogenic muscle atrophy, especially in the lower limbs | 0.2 | HPO |
7415 | VCP | C1847584 | Distal sensory impairment | 0.2 | HPO |
7415 | VCP | C1847766 | Shoulder girdle muscle atrophy | 0.2 | HPO |
7415 | VCP | C1848207 | Poor speech | 0.2 | HPO |
7415 | VCP | C1848736 | Distal amyotrophy | 0.2 | HPO |
7415 | VCP | C1849134 | Decreased lower limb vibratory sense | 0.2 | HPO |
7415 | VCP | C1853932 | Rimmed vacuoles on biopsy | 0.2 | HPO |
7415 | VCP | C1854657 | Limb fasciculations | 0.2 | HPO |
7415 | VCP | C1864696 | Distal limb muscle weakness due to peripheral neuropathy | 0.2 | HPO |
7415 | VCP | C1866772 | Abnormal nerve conduction velocity | 0.2 | HPO |
7415 | VCP | C2675334 | Restrictive behavior, interests, and activities | 0.2 | HPO |
7415 | VCP | C2700617 | Irritation - emotion | 0.2 | HPO |
7415 | VCP | C3151403 | AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA | 0.2 | UNIPROT |
7415 | VCP | C3887611 | Restlessness | 0.2 | HPO |
7415 | VCP | C4011788 | Behavioral variant of frontotemporal dementia | 0.2 | ORPHANET |
7415 | VCP | C4020847 | Abnormality of pelvic girdle bone morphology | 0.2 | HPO |
7415 | VCP | C4020851 | Cortical white matter abnormalities seen on MRI | 0.2 | HPO |
7415 | VCP | C4020854 | Neuro-degenerative disease | 0.2 | HPO |
7415 | VCP | C4020871 | Dystonic disease | 0.2 | HPO |
7415 | VCP | C4020884 | Anxiety disease | 0.2 | HPO |
7415 | VCP | C4021528 | Pelvic girdle amyotrophy | 0.2 | HPO |
7415 | VCP | C4021584 | Frontotemporal cerebral atrophy | 0.2 | HPO |
7415 | VCP | C4021727 | EMG: neuropathic changes | 0.2 | HPO |
7415 | VCP | C4021799 | Restrictive behavior | 0.2 | HPO |
7415 | VCP | C4022587 | Fatigable weakness of respiratory muscles | 0.2 | HPO |
7415 | VCP | C4022588 | Fatigable weakness of swallowing muscles | 0.2 | HPO |
7415 | VCP | C4022798 | Abnormal brain FDG positron emission tomography | 0.2 | HPO |
7415 | VCP | C4023470 | EEG with continuous slow activity | 0.2 | HPO |
7415 | VCP | C4024936 | Temporal cortical atrophy | 0.2 | HPO |
7415 | VCP | C4024956 | Grammar-specific speech disorder | 0.2 | HPO |
7415 | VCP | C4024965 | Frontal cortical atrophy | 0.2 | HPO |
7415 | VCP | C4072849 | Scapular weakness | 0.2 | HPO |
7415 | VCP | C4072928 | Spoken Word Recognition Deficit | 0.2 | HPO |
7415 | VCP | C4280380 | Repeated speech | 0.2 | HPO |
7415 | VCP | C4280574 | Problems speaking | 0.2 | HPO |
7415 | VCP | C4280576 | Difficulty making arithmetical calculations | 0.2 | HPO |
7415 | VCP | C0029401 | Osteitis Deformans | 0.0230339837419487 | BEFREE;LHGDN |
7415 | VCP | C0497327 | Dementia | 0.0147778248382384 | BEFREE;LHGDN |
7415 | VCP | C0236642 | Pick Disease of the Brain | 0.0126374320738026 | BEFREE |
7415 | VCP | C0027627 | Neoplasm Metastasis | 0.00575490709115785 | BEFREE;LHGDN |
7415 | VCP | C0011265 | Presenile dementia | 0.0038461749789834 | BEFREE |
7415 | VCP | C0029463 | Osteosarcoma | 0.00328236603323995 | BEFREE;LHGDN |
7415 | VCP | C0751072 | Frontotemporal Lobar Degeneration | 0.0030219946263441 | BEFREE |
7415 | VCP | C0024408 | Machado-Joseph Disease | 0.00300763924902685 | BEFREE;LHGDN |
7415 | VCP | C0009404 | Colorectal Neoplasms | 0.00273291246481375 | LHGDN |
7415 | VCP | C0010674 | Cystic Fibrosis | 0.00273291246481375 | LHGDN |
7415 | VCP | C0023418 | leukemia | 0.00273291246481375 | LHGDN |
7415 | VCP | C0006142 | Malignant neoplasm of breast | 0.0026817553075011 | BEFREE;GAD |
7415 | VCP | C1853926 | NONAKA MYOPATHY | 0.0021978142737048 | BEFREE |
7415 | VCP | C1862941 | Amyotrophic Lateral Sclerosis, Sporadic | 0.0016483607052786 | BEFREE |
7415 | VCP | C1368019 | Paget Disease | 0.0013736339210655 | BEFREE |
7415 | VCP | C3899989 | Autosomal Dominant Disorder | 0.0013736339210655 | BEFREE |
7415 | VCP | C0025202 | melanoma | 0.0010989071368524 | BEFREE |
7415 | VCP | C0030552 | Paresis | 0.0010989071368524 | BEFREE |
7415 | VCP | C0035334 | Retinitis Pigmentosa | 0.0010989071368524 | BEFREE |
7415 | VCP | C0085084 | Motor Neuron Disease | 0.0010989071368524 | BEFREE |
7415 | VCP | C0678222 | Breast Carcinoma | 0.0010989071368524 | BEFREE |
7415 | VCP | C1285162 | Degenerative disorder | 0.0010989071368524 | BEFREE |
7415 | VCP | C0007131 | Non-Small Cell Lung Carcinoma | 0.0008241803526393 | BEFREE |
7415 | VCP | C0027831 | Neurofibromatosis 1 | 0.0008241803526393 | BEFREE |
7415 | VCP | C0030567 | Parkinson Disease | 0.0008241803526393 | BEFREE |
7415 | VCP | C0302592 | Cervix carcinoma | 0.0008241803526393 | BEFREE |
7415 | VCP | C0338656 | Impaired cognition | 0.0008241803526393 | BEFREE |
7415 | VCP | C1843792 | FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED | 0.0008241803526393 | BEFREE |
7415 | VCP | C2239176 | Liver carcinoma | 0.0008241803526393 | BEFREE |
7415 | VCP | C2931820 | Inclusion body myopathy, autosomal dominant | 0.0008241803526393 | BEFREE |
7415 | VCP | C3811918 | GRN-related frontotemporal dementia | 0.0008241803526393 | BEFREE |
7415 | VCP | C0002395 | Alzheimer's Disease | 0.0005494535684262 | BEFREE |
7415 | VCP | C0037773 | Spastic Paraplegia, Hereditary | 0.0005494535684262 | BEFREE |
7415 | VCP | C0153676 | Secondary malignant neoplasm of lung | 0.0005494535684262 | BEFREE |
7415 | VCP | C0376358 | Malignant neoplasm of prostate | 0.0005494535684262 | BEFREE |
7415 | VCP | C0585442 | Osteosarcoma of bone | 0.0005494535684262 | BEFREE |
7415 | VCP | C0596263 | Carcinogenesis | 0.0005494535684262 | BEFREE |
7415 | VCP | C0600139 | Prostate carcinoma | 0.0005494535684262 | BEFREE |
7415 | VCP | C0686619 | Secondary malignant neoplasm of lymph node | 0.0005494535684262 | BEFREE |
7415 | VCP | C0699791 | Stomach Carcinoma | 0.0005494535684262 | BEFREE |
7415 | VCP | C2718017 | TDP-43 Proteinopathies | 0.0005494535684262 | BEFREE |
7415 | VCP | C2931230 | Vacuolar myopathy | 0.0005494535684262 | BEFREE |
7415 | VCP | C4024896 | Motor neuron atrophy | 0.0005494535684262 | BEFREE |
7415 | VCP | C0002726 | Amyloidosis | 0.0002747267842131 | BEFREE |
7415 | VCP | C0005940 | Bone Diseases | 0.0002747267842131 | BEFREE |
7415 | VCP | C0006625 | Cachexia | 0.0002747267842131 | BEFREE |
7415 | VCP | C0007121 | Bronchogenic Carcinoma | 0.0002747267842131 | BEFREE |
7415 | VCP | C0007137 | Squamous cell carcinoma | 0.0002747267842131 | BEFREE |
7415 | VCP | C0007847 | Malignant tumor of cervix | 0.0002747267842131 | BEFREE |
7415 | VCP | C0007959 | Charcot-Marie-Tooth Disease | 0.0002747267842131 | BEFREE |
7415 | VCP | C0008073 | Developmental Disabilities | 0.0002747267842131 | BEFREE |
7415 | VCP | C0009241 | Cognition Disorders | 0.0002747267842131 | BEFREE |
7415 | VCP | C0009402 | Colorectal Carcinoma | 0.0002747267842131 | BEFREE |
7415 | VCP | C0014544 | Epilepsy | 0.0002747267842131 | BEFREE |
7415 | VCP | C0019348 | Herpes Simplex Infections | 0.0002747267842131 | BEFREE |
7415 | VCP | C0023493 | Adult T-Cell Lymphoma/Leukemia | 0.0002747267842131 | BEFREE |
7415 | VCP | C0024117 | Chronic Obstructive Airway Disease | 0.0002747267842131 | BEFREE |
7415 | VCP | C0027765 | nervous system disorder | 0.0002747267842131 | BEFREE |
7415 | VCP | C0027868 | Neuromuscular Diseases | 0.0002747267842131 | BEFREE |
7415 | VCP | C0029925 | Ovarian Carcinoma | 0.0002747267842131 | BEFREE |
7415 | VCP | C0032285 | Pneumonia | 0.0002747267842131 | BEFREE |
7415 | VCP | C0033626 | Protein Deficiency | 0.0002747267842131 | BEFREE |
7415 | VCP | C0034067 | Pulmonary Emphysema | 0.0002747267842131 | BEFREE |
7415 | VCP | C0034152 | Henoch-Schoenlein Purpura | 0.0002747267842131 | BEFREE |
7415 | VCP | C0152013 | Adenocarcinoma of lung (disorder) | 0.0002747267842131 | BEFREE |
7415 | VCP | C0152018 | Esophageal carcinoma | 0.0002747267842131 | BEFREE |
7415 | VCP | C0153594 | Malignant neoplasm of testis | 0.0002747267842131 | BEFREE |
7415 | VCP | C0206659 | Embryonal Carcinoma | 0.0002747267842131 | BEFREE |
7415 | VCP | C0206708 | Cervical Intraepithelial Neoplasia | 0.0002747267842131 | BEFREE |
7415 | VCP | C0220620 | Gastrointestinal Carcinoid Tumor | 0.0002747267842131 | BEFREE |
7415 | VCP | C0235025 | Peripheral motor neuropathy | 0.0002747267842131 | BEFREE |
7415 | VCP | C0235974 | Pancreatic carcinoma | 0.0002747267842131 | BEFREE |
7415 | VCP | C0238190 | Inclusion Body Myositis (disorder) | 0.0002747267842131 | BEFREE |
7415 | VCP | C0242422 | Parkinsonian Disorders | 0.0002747267842131 | BEFREE |
7415 | VCP | C0264733 | Ventricular dilatation (disorder) | 0.0002747267842131 | BEFREE |
7415 | VCP | C0266999 | Vesicular Stomatitis | 0.0002747267842131 | BEFREE |
7415 | VCP | C0268398 | Familial lichen amyloidosis | 0.0002747267842131 | BEFREE |
7415 | VCP | C0270914 | Hereditary Motor and Sensory-Neuropathy Type II | 0.0002747267842131 | BEFREE |
7415 | VCP | C0279626 | Squamous cell carcinoma of esophagus | 0.0002747267842131 | BEFREE |
7415 | VCP | C0280313 | Squamous cell carcinoma of oropharynx | 0.0002747267842131 | BEFREE |
7415 | VCP | C0282513 | Primary Progressive Aphasia (disorder) | 0.0002747267842131 | BEFREE |
7415 | VCP | C0346647 | Malignant neoplasm of pancreas | 0.0002747267842131 | BEFREE |
7415 | VCP | C0391957 | idiopathic epilepsy | 0.0002747267842131 | BEFREE |
7415 | VCP | C0410198 | Proximal myopathy | 0.0002747267842131 | BEFREE |
7415 | VCP | C0494463 | Alzheimer Disease, Late Onset | 0.0002747267842131 | BEFREE |
7415 | VCP | C0521158 | Recurrent tumor | 0.0002747267842131 | BEFREE |
7415 | VCP | C0677886 | Epithelial ovarian cancer | 0.0002747267842131 | BEFREE |
7415 | VCP | C0751265 | Learning Disabilities | 0.0002747267842131 | BEFREE |
7415 | VCP | C0751336 | Distal Muscular Dystrophies | 0.0002747267842131 | BEFREE |
7415 | VCP | C0751337 | X-Linked Emery-Dreifuss Muscular Dystrophy | 0.0002747267842131 | BEFREE |
7415 | VCP | C0855197 | Testicular malignant germ cell tumor | 0.0002747267842131 | BEFREE |
7415 | VCP | C0878544 | Cardiomyopathies | 0.0002747267842131 | BEFREE |
7415 | VCP | C0917981 | Progressive Muscular Atrophy | 0.0002747267842131 | BEFREE |
7415 | VCP | C1370419 | Granulosa cell tumor of the ovary | 0.0002747267842131 | BEFREE |
7415 | VCP | C1395088 | Nervous system--Degeneration | 0.0002747267842131 | BEFREE |
7415 | VCP | C1458155 | Mammary Neoplasms | 0.0002747267842131 | BEFREE |
7415 | VCP | C1527249 | Colorectal Cancer | 0.0002747267842131 | BEFREE |
7415 | VCP | C1833373 | Inclusion Body Myopathy, Autosomal Recessive | 0.0002747267842131 | BEFREE |
7415 | VCP | C2931822 | Nasopharyngeal carcinoma | 0.0002747267842131 | BEFREE |
7415 | VCP | C3266164 | Dropped head syndrome | 0.0002747267842131 | BEFREE |
7415 | VCP | C3887505 | DYSFUNCTION - SKIN DISORDERS | 0.0002747267842131 | BEFREE |
7415 | VCP | C4020732 | Mitochondrial abnormalities | 0.0002747267842131 | BEFREE |
7415 | VCP | C4048328 | cervical cancer | 0.0002747267842131 | BEFREE |