* We recommend a score >= 0.08 for meaningful Gene-Disease associations

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
1785	DNM2	C1834558	Myopathy, Centronuclear, Autosomal Dominant	0.683846174978983	BEFREE;CTD_human;MGD;ORPHANET;UNIPROT
1785	DNM2	C1847902	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder)	0.600274726784213	BEFREE;CTD_human;ORPHANET;UNIPROT
1785	DNM2	C3809272	LETHAL CONGENITAL CONTRACTURE SYNDROME 5	0.4	ORPHANET;UNIPROT
1785	DNM2	C0752282	Congenital Structural Myopathy	0.208473464178654	BEFREE;CTD_human;LHGDN
1785	DNM2	C0005745	Blepharoptosis	0.200274726784213	BEFREE;HPO
1785	DNM2	C0009917	Contracture	0.200274726784213	BEFREE;HPO
1785	DNM2	C0728829	Congenital pes cavus	0.200274726784213	BEFREE;HPO
1785	DNM2	C0009918	Contracture of joint	0.2	HPO
1785	DNM2	C0020224	Polyhydramnios	0.2	HPO
1785	DNM2	C0024032	Low Birth Weights	0.2	HPO
1785	DNM2	C0026827	Muscle hypotonia	0.2	HPO
1785	DNM2	C0035229	Respiratory Insufficiency	0.2	HPO
1785	DNM2	C0035317	Retinal Hemorrhage	0.2	HPO
1785	DNM2	C0151576	Elevated creatine kinase	0.2	HPO
1785	DNM2	C0162292	External Ophthalmoplegia	0.2	HPO
1785	DNM2	C0162674	Chronic progressive external ophthalmoplegia	0.2	HPO
1785	DNM2	C0221629	Proximal muscle weakness	0.2	HPO
1785	DNM2	C0234146	Absent reflex	0.2	HPO
1785	DNM2	C0235659	Reduced fetal movement	0.2	HPO
1785	DNM2	C0235991	Small for gestational age (disorder)	0.2	HPO
1785	DNM2	C0241005	Creatine phosphokinase serum increased	0.2	HPO
1785	DNM2	C0241772	Reflex, Deep Tendon, Absent	0.2	HPO
1785	DNM2	C0278124	Absent tendon reflex	0.2	HPO
1785	DNM2	C0332878	Congenital joint contractures	0.2	HPO
1785	DNM2	C0333068	Flexion contracture	0.2	HPO
1785	DNM2	C0376175	Bell Palsy	0.2	HPO
1785	DNM2	C0424585	Tires quickly	0.2	HPO
1785	DNM2	C0426818	Thin rib	0.2	HPO
1785	DNM2	C0427055	Facial Paresis	0.2	HPO
1785	DNM2	C0427065	Distal muscle weakness	0.2	HPO
1785	DNM2	C0700078	Decreased tendon reflex	0.2	HPO
1785	DNM2	C1837098	Easy fatigability	0.2	HPO
1785	DNM2	C1837496	Axonal degeneration	0.2	HPO
1785	DNM2	C1838869	Proximal neurogenic muscle weakness	0.2	HPO
1785	DNM2	C1842170	Centrally nucleated skeletal muscle fibers	0.2	HPO
1785	DNM2	C1843077	Segmental demyelination/remyelination	0.2	HPO
1785	DNM2	C1844947	Death in early childhood	0.2	HPO
1785	DNM2	C1847584	Distal sensory impairment	0.2	HPO
1785	DNM2	C1847906	Onion bulb formation	0.2	HPO
1785	DNM2	C1848736	Distal amyotrophy	0.2	HPO
1785	DNM2	C1850530	Flexion contractures of joints	0.2	HPO
1785	DNM2	C1854301	Motor delay	0.2	HPO
1785	DNM2	C1854494	Slow progression	0.2	HPO
1785	DNM2	C1858285	Decreased number of large and small myelinated fibers	0.2	HPO
1785	DNM2	C1858430	Death in infancy	0.2	HPO
1785	DNM2	C1858719	Facial muscle weakness of muscles innervated by CN VII	0.2	HPO
1785	DNM2	C1864696	Distal limb muscle weakness due to peripheral neuropathy	0.2	HPO
1785	DNM2	C2752013	Prenatal onset	0.2	HPO
1785	DNM2	C4020855	Respiratory function loss	0.2	HPO
1785	DNM2	C4020874	No development of motor milestones	0.2	HPO
1785	DNM2	C4020899	Autosomal recessive predisposition	0.2	HPO
1785	DNM2	C4025214	Sleepy facial expression	0.2	HPO
1785	DNM2	C3149841	POLYCYSTIC KIDNEY DISEASE 1	0.08	MGD
1785	DNM2	C0007959	Charcot-Marie-Tooth Disease	0.0109603606138895	BEFREE;LHGDN
1785	DNM2	C0175709	Centronuclear myopathy	0.0087912570948192	BEFREE
1785	DNM2	C0002395	Alzheimer's Disease	0.0084223070213417	BEFREE;GAD;LHGDN
1785	DNM2	C0006142	Malignant neoplasm of breast	0.0032312088759273	BEFREE;GAD
1785	DNM2	C0027627	Neoplasm Metastasis	0.002747267842131	BEFREE
1785	DNM2	C0442874	Neuropathy	0.002747267842131	BEFREE
1785	DNM2	C3714514	Infection	0.00273291246481375	LHGDN
1785	DNM2	C0013264	Muscular Dystrophy, Duchenne	0.0019230874894917	BEFREE
1785	DNM2	C0026848	Myopathy	0.0019230874894917	BEFREE
1785	DNM2	C0020538	Hypertensive disease	0.0013736339210655	BEFREE
1785	DNM2	C0031117	Peripheral Neuropathy	0.0013736339210655	BEFREE
1785	DNM2	C0027868	Neuromuscular Diseases	0.0010989071368524	BEFREE
1785	DNM2	C0178874	Tumor Progression	0.0008241803526393	BEFREE
1785	DNM2	C0235974	Pancreatic carcinoma	0.0008241803526393	BEFREE
1785	DNM2	C0346647	Malignant neoplasm of pancreas	0.0008241803526393	BEFREE
1785	DNM2	C0410203	X-linked centronuclear myopathy	0.0008241803526393	BEFREE
1785	DNM2	C0678222	Breast Carcinoma	0.0008241803526393	BEFREE
1785	DNM2	C0017636	Glioblastoma	0.0005494535684262	BEFREE
1785	DNM2	C0030552	Paresis	0.0005494535684262	BEFREE
1785	DNM2	C0085580	Essential Hypertension	0.0005494535684262	BEFREE
1785	DNM2	C0086543	Cataract	0.0005494535684262	BEFREE
1785	DNM2	C0151786	Muscle Weakness	0.0005494535684262	BEFREE
1785	DNM2	C0270914	Hereditary Motor and Sensory-Neuropathy Type II	0.0005494535684262	BEFREE
1785	DNM2	C0376358	Malignant neoplasm of prostate	0.0005494535684262	BEFREE
1785	DNM2	C0521707	Bilateral cataracts (disorder)	0.0005494535684262	BEFREE
1785	DNM2	C0524851	Neurodegenerative Disorders	0.0005494535684262	BEFREE
1785	DNM2	C0600139	Prostate carcinoma	0.0005494535684262	BEFREE
1785	DNM2	C0686619	Secondary malignant neoplasm of lymph node	0.0005494535684262	BEFREE
1785	DNM2	C0699790	Colon Carcinoma	0.0005494535684262	BEFREE
1785	DNM2	C1449563	Cardiomyopathy, Familial Idiopathic	0.0005494535684262	BEFREE
1785	DNM2	C1833219	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder)	0.0005494535684262	BEFREE
1785	DNM2	C2239176	Liver carcinoma	0.0005494535684262	BEFREE
1785	DNM2	C3887505	DYSFUNCTION - SKIN DISORDERS	0.0005494535684262	BEFREE
1785	DNM2	C0000768	Congenital Abnormality	0.0002747267842131	BEFREE
1785	DNM2	C0001430	Adenoma	0.0002747267842131	BEFREE
1785	DNM2	C0001486	Adenovirus Infections	0.0002747267842131	BEFREE
1785	DNM2	C0002736	Amyotrophic Lateral Sclerosis	0.0002747267842131	BEFREE
1785	DNM2	C0003467	Anxiety	0.0002747267842131	BEFREE
1785	DNM2	C0003469	Anxiety Disorders	0.0002747267842131	BEFREE
1785	DNM2	C0004114	Astrocytoma	0.0002747267842131	BEFREE
1785	DNM2	C0004364	Autoimmune Diseases	0.0002747267842131	BEFREE
1785	DNM2	C0007102	Malignant tumor of colon	0.0002747267842131	BEFREE
1785	DNM2	C0007113	Rectal Carcinoma	0.0002747267842131	BEFREE
1785	DNM2	C0007194	Hypertrophic Cardiomyopathy	0.0002747267842131	BEFREE
1785	DNM2	C0008055	Chikungunya Fever	0.0002747267842131	BEFREE
1785	DNM2	C0009324	Ulcerative Colitis	0.0002747267842131	BEFREE
1785	DNM2	C0011265	Presenile dementia	0.0002747267842131	BEFREE
1785	DNM2	C0011847	Diabetes	0.0002747267842131	BEFREE
1785	DNM2	C0011849	Diabetes Mellitus	0.0002747267842131	BEFREE
1785	DNM2	C0017638	Glioma	0.0002747267842131	BEFREE
1785	DNM2	C0018801	Heart failure	0.0002747267842131	BEFREE
1785	DNM2	C0018802	Congestive heart failure	0.0002747267842131	BEFREE
1785	DNM2	C0019163	Hepatitis B	0.0002747267842131	BEFREE
1785	DNM2	C0023434	Chronic Lymphocytic Leukemia	0.0002747267842131	BEFREE
1785	DNM2	C0023449	Acute lymphocytic leukemia	0.0002747267842131	BEFREE
1785	DNM2	C0023530	Leukopenia	0.0002747267842131	BEFREE
1785	DNM2	C0023976	Long QT Syndrome	0.0002747267842131	BEFREE
1785	DNM2	C0024623	Malignant neoplasm of stomach	0.0002747267842131	BEFREE
1785	DNM2	C0025149	Medulloblastoma	0.0002747267842131	BEFREE
1785	DNM2	C0025517	Metabolic Diseases	0.0002747267842131	BEFREE
1785	DNM2	C0027765	nervous system disorder	0.0002747267842131	BEFREE
1785	DNM2	C0027947	Neutropenia	0.0002747267842131	BEFREE
1785	DNM2	C0029925	Ovarian Carcinoma	0.0002747267842131	BEFREE
1785	DNM2	C0030297	Pancreatic Neoplasm	0.0002747267842131	BEFREE
1785	DNM2	C0033377	Ptosis	0.0002747267842131	BEFREE
1785	DNM2	C0036341	Schizophrenia	0.0002747267842131	BEFREE
1785	DNM2	C0040485	Torticollis	0.0002747267842131	BEFREE
1785	DNM2	C0042373	Vascular Diseases	0.0002747267842131	BEFREE
1785	DNM2	C0043194	Wiskott-Aldrich Syndrome	0.0002747267842131	BEFREE
1785	DNM2	C0085623	Akinesia	0.0002747267842131	BEFREE
1785	DNM2	C0151313	Sensory neuropathy	0.0002747267842131	BEFREE
1785	DNM2	C0175778	Larsen syndrome	0.0002747267842131	BEFREE
1785	DNM2	C0268398	Familial lichen amyloidosis	0.0002747267842131	BEFREE
1785	DNM2	C0270921	Axonal neuropathy	0.0002747267842131	BEFREE
1785	DNM2	C0270960	Congenital myopathy (disorder)	0.0002747267842131	BEFREE
1785	DNM2	C0271682	Mixed sensory-motor polyneuropathy	0.0002747267842131	BEFREE
1785	DNM2	C0279671	Cervical Squamous Cell Carcinoma	0.0002747267842131	BEFREE
1785	DNM2	C0302592	Cervix carcinoma	0.0002747267842131	BEFREE
1785	DNM2	C0339277	Corneal Dystrophy, Juvenile Epithelial of Meesmann	0.0002747267842131	BEFREE
1785	DNM2	C0410204	Myopathy, Centronuclear, Autosomal Recessive	0.0002747267842131	BEFREE
1785	DNM2	C0424295	Hyperactive behavior	0.0002747267842131	BEFREE
1785	DNM2	C0494463	Alzheimer Disease, Late Onset	0.0002747267842131	BEFREE
1785	DNM2	C0497327	Dementia	0.0002747267842131	BEFREE
1785	DNM2	C0497552	Congenital neurologic anomalies	0.0002747267842131	BEFREE
1785	DNM2	C0549473	Thyroid carcinoma	0.0002747267842131	BEFREE
1785	DNM2	C0596263	Carcinogenesis	0.0002747267842131	BEFREE
1785	DNM2	C0598766	Leukemogenesis	0.0002747267842131	BEFREE
1785	DNM2	C0699791	Stomach Carcinoma	0.0002747267842131	BEFREE
1785	DNM2	C0751951	Central Core Myopathy (disorder)	0.0002747267842131	BEFREE
1785	DNM2	C0795953	MASA SYNDROME (disorder)	0.0002747267842131	BEFREE
1785	DNM2	C0917713	Becker Muscular Dystrophy	0.0002747267842131	BEFREE
1785	DNM2	C1140680	Malignant neoplasm of ovary	0.0002747267842131	BEFREE
1785	DNM2	C1285162	Degenerative disorder	0.0002747267842131	BEFREE
1785	DNM2	C1458155	Mammary Neoplasms	0.0002747267842131	BEFREE
1785	DNM2	C1721006	Keratoderma, Palmoplantar, Epidermolytic	0.0002747267842131	BEFREE
1785	DNM2	C1842237	Charcot-Marie-Tooth Disease, Dominant Intermediate C	0.0002747267842131	BEFREE
1785	DNM2	C1850808	Miyoshi myopathy	0.0002747267842131	BEFREE
1785	DNM2	C1869123	Limb-girdle muscular dystrophy type 2A	0.0002747267842131	BEFREE
1785	DNM2	C1960469	Left ventricular noncompaction	0.0002747267842131	BEFREE
1785	DNM2	C1961102	Precursor Cell Lymphoblastic Leukemia Lymphoma	0.0002747267842131	BEFREE
1785	DNM2	C2932678	Inherited Peripheral Neuropathy	0.0002747267842131	BEFREE
1785	DNM2	C3542021	Duchenne and Becker Muscular Dystrophy	0.0002747267842131	BEFREE
1785	DNM2	C3645536	Autosomal Recessive Centronuclear Myopathy	0.0002747267842131	BEFREE