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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
4137	MAPT	C0338451	Frontotemporal dementia	0.701663256709592	BEFREE;CTD_human;GAD;HPO;UNIPROT
4137	MAPT	C0038868	Progressive supranuclear palsy	0.679659466874971	BEFREE;CTD_human;GAD;LHGDN;ORPHANET;UNIPROT
4137	MAPT	C0497327	Dementia	0.513123446601814	BEFREE;CTD_human;GAD;HPO;LHGDN
4137	MAPT	C0236642	Pick Disease of the Brain	0.461249717502204	BEFREE;CTD_human;LHGDN;UNIPROT
4137	MAPT	C0242422	Parkinsonian Disorders	0.447607749522594	BEFREE;CTD_human;GAD;HPO;LHGDN
4137	MAPT	C0002395	Alzheimer's Disease	0.412954627512336	BEFREE;CTD_human;GAD;LHGDN
4137	MAPT	C1850077	Supranuclear Palsy, Progressive, 1, Atypical	0.400274726784213	BEFREE;CTD_human;ORPHANET
4137	MAPT	C0030567	Parkinson Disease	0.323045972857553	BEFREE;CTD_human;GAD;LHGDN
4137	MAPT	C0949664	Tauopathies	0.292242834902753	BEFREE;CTD_human;GAD;LHGDN
4137	MAPT	C0524851	Neurodegenerative Disorders	0.279345031422054	BEFREE;CTD_human;GAD;LHGDN
4137	MAPT	C0002736	Amyotrophic Lateral Sclerosis	0.208161935614446	BEFREE;GAD;HPO;LHGDN
4137	MAPT	C0009241	Cognition Disorders	0.203021994626344	BEFREE;CTD_human
4137	MAPT	C0025261	Memory Disorders	0.202407028523288	CTD_human;GAD
4137	MAPT	C4011788	Behavioral variant of frontotemporal dementia	0.201923087489492	BEFREE;ORPHANET
4137	MAPT	C0338462	Semantic Dementia	0.201373633921065	BEFREE;ORPHANET
4137	MAPT	C3160718	PARKINSON DISEASE, LATE-ONSET	0.201373633921065	BEFREE;CTD_human
4137	MAPT	C0233794	Memory impairment	0.201373633921065	BEFREE;HPO
4137	MAPT	C0240735	Personality change	0.200824180352639	BEFREE;HPO
4137	MAPT	C0751295	Memory Loss	0.200824180352639	BEFREE;HPO
4137	MAPT	C0751706	Primary Progressive Nonfluent Aphasia	0.200824180352639	BEFREE;ORPHANET
4137	MAPT	C0026837	Muscle Rigidity	0.200824180352639	BEFREE;HPO
4137	MAPT	C0040822	Tremor	0.200824180352639	BEFREE;HPO
4137	MAPT	C0005586	Bipolar Disorder	0.200274726784213	BEFREE;PSYGENET
4137	MAPT	C0011581	Depressive disorder	0.200274726784213	BEFREE;HPO
4137	MAPT	C0233565	Bradykinesia	0.200274726784213	BEFREE;HPO
4137	MAPT	C0333454	Granulovacuolar degeneration	0.2	HPO
4137	MAPT	C0338455	Dementia of frontal lobe type	0.2	HPO
4137	MAPT	C0344232	Blurred vision	0.2	HPO
4137	MAPT	C0424290	Compulsive hoarding	0.2	HPO
4137	MAPT	C0424296	Social disinhibition	0.2	HPO
4137	MAPT	C0424304	Inappropriate laughter	0.2	HPO
4137	MAPT	C0424323	Physical aggression	0.2	HPO
4137	MAPT	C0474420	Inappropriate sexual behavior	0.2	HPO
4137	MAPT	C0476254	Dyslexia	0.2	HPO
4137	MAPT	C0542223	Loss of speech	0.2	HPO
4137	MAPT	C0542476	Forgetful	0.2	HPO
4137	MAPT	C0575158	Kyphoscoliosis deformity of spine	0.2	HPO
4137	MAPT	C0751401	Ophthalmoparesis	0.2	HPO
4137	MAPT	C0948163	Leukoaraiosis	0.2	HPO
4137	MAPT	C0973461	Dysphasia	0.2	HPO
4137	MAPT	C1142448	Apraxia of eyelid	0.2	HPO
4137	MAPT	C1262477	Weight decreased	0.2	CTD_human
4137	MAPT	C1411876	Developmental arithmetic disorder	0.2	HPO
4137	MAPT	C1457883	Aggressive reaction	0.2	HPO
4137	MAPT	C1720037	Supranuclear gaze palsy	0.2	HPO
4137	MAPT	C1836149	Axial dystonia	0.2	HPO
4137	MAPT	C1836150	Gait imbalance	0.2	HPO
4137	MAPT	C1836151	Frontolimbic dementia	0.2	HPO
4137	MAPT	C1836940	Excess nuchal skin	0.2	HPO
4137	MAPT	C1838319	Primitive reflexes (palmomental, snout, glabellar)	0.2	HPO
4137	MAPT	C1838320	Hyperorality	0.2	HPO
4137	MAPT	C1848207	Poor speech	0.2	HPO
4137	MAPT	C1850496	Neuronal loss	0.2	HPO
4137	MAPT	C1853237	Isolated cases	0.2	HPO
4137	MAPT	C1853562	Adult onset	0.2	HPO
4137	MAPT	C2675334	Restrictive behavior, interests, and activities	0.2	HPO
4137	MAPT	C2700617	Irritation - emotion	0.2	HPO
4137	MAPT	C3887611	Restlessness	0.2	HPO
4137	MAPT	C3887612	Psychomotor Agitation	0.2	CTD_human
4137	MAPT	C3887667	Retrocollis	0.2	HPO
4137	MAPT	C4020851	Cortical white matter abnormalities seen on MRI	0.2	HPO
4137	MAPT	C4020859	Pyramidal tract disease	0.2	HPO
4137	MAPT	C4020884	Anxiety disease	0.2	HPO
4137	MAPT	C4020887	Photodysphoria	0.2	HPO
4137	MAPT	C4021584	Frontotemporal cerebral atrophy	0.2	HPO
4137	MAPT	C4021761	Morphological abnormality of the pyramidal tract	0.2	HPO
4137	MAPT	C4021799	Restrictive behavior	0.2	HPO
4137	MAPT	C4022798	Abnormal brain FDG positron emission tomography	0.2	HPO
4137	MAPT	C4023470	EEG with continuous slow activity	0.2	HPO
4137	MAPT	C4024936	Temporal cortical atrophy	0.2	HPO
4137	MAPT	C4024956	Grammar-specific speech disorder	0.2	HPO
4137	MAPT	C4072928	Spoken Word Recognition Deficit	0.2	HPO
4137	MAPT	C4280380	Repeated speech	0.2	HPO
4137	MAPT	C4280574	Problems speaking	0.2	HPO
4137	MAPT	C4280576	Difficulty making arithmetical calculations	0.2	HPO
4137	MAPT	C0001807	Aggressive behavior	0.2	HPO
4137	MAPT	C0002018	Alexia	0.2	HPO
4137	MAPT	C0003467	Anxiety	0.2	HPO
4137	MAPT	C0003635	Apraxias	0.2	HPO
4137	MAPT	C0011168	Deglutition Disorders	0.2	HPO
4137	MAPT	C0012569	Diplopia	0.2	HPO
4137	MAPT	C0013362	Dysarthria	0.2	HPO
4137	MAPT	C0013528	Echolalia	0.2	HPO
4137	MAPT	C0017639	Gliosis	0.2	HPO
4137	MAPT	C0020505	Hyperphagia	0.2	HPO
4137	MAPT	C0023015	Language Disorders	0.2	HPO
4137	MAPT	C0023186	Learning Disorders	0.2	CTD_human
4137	MAPT	C0026884	Mutism	0.2	HPO
4137	MAPT	C0035229	Respiratory Insufficiency	0.2	CTD_human
4137	MAPT	C0038002	Splenomegaly	0.2	CTD_human
4137	MAPT	C0038271	Stereotyped Behavior	0.2	HPO
4137	MAPT	C0038273	Stereotypic Movement Disorder	0.2	HPO
4137	MAPT	C0085400	Neurofibrillary degeneration (morphologic abnormality)	0.2	HPO
4137	MAPT	C0085623	Akinesia	0.2	HPO
4137	MAPT	C0085632	Apathy	0.2	HPO
4137	MAPT	C0085636	Photophobia	0.2	HPO
4137	MAPT	C0232461	Increased appetite (finding)	0.2	HPO
4137	MAPT	C0234132	Pyramidal sign	0.2	HPO
4137	MAPT	C0234144	Dysgraphia	0.2	HPO
4137	MAPT	C0002726	Amyloidosis	0.0326126194094118	BEFREE;GAD;LHGDN
4137	MAPT	C0011265	Presenile dementia	0.0156594267001467	BEFREE
4137	MAPT	C0751072	Frontotemporal Lobar Degeneration	0.0136708266760251	BEFREE;GAD
4137	MAPT	C3887505	DYSFUNCTION - SKIN DISORDERS	0.0098901642316716	BEFREE
4137	MAPT	C0013080	Down Syndrome	0.00902291774708056	BEFREE;LHGDN
4137	MAPT	C0333463	Senile Plaques	0.0076923499579668	BEFREE
4137	MAPT	C0393570	Corticobasal degeneration	0.0074176231737537	BEFREE
4137	MAPT	C0022336	Creutzfeldt-Jakob disease	0.00651357490916725	BEFREE;GAD;LHGDN
4137	MAPT	C0338656	Impaired cognition	0.0063187160369013	BEFREE
4137	MAPT	C0282513	Primary Progressive Aphasia (disorder)	0.0056382373992153	BEFREE;GAD
4137	MAPT	C0027051	Myocardial Infarction	0.00513994098810175	GAD;LHGDN
4137	MAPT	C0036341	Schizophrenia	0.004814057046576	GAD
4137	MAPT	C0026650	Movement Disorders	0.0043301160127797	BEFREE;GAD
4137	MAPT	C3811918	GRN-related frontotemporal dementia	0.0041209017631965	BEFREE
4137	MAPT	C3887938	COLORBLINDNESS, PARTIAL, DEUTAN SERIES	0.0041209017631965	BEFREE
4137	MAPT	C0162534	Prion Diseases	0.00355709281745305	BEFREE;LHGDN
4137	MAPT	C2936349	Plaque, Amyloid	0.0032967214105572	BEFREE
4137	MAPT	C0026769	Multiple Sclerosis	0.00300763924902685	BEFREE;LHGDN
4137	MAPT	C0333641	Atrophic	0.00273291246481375	LHGDN
4137	MAPT	C0393571	Multiple System Atrophy	0.00273291246481375	LHGDN
4137	MAPT	C3714514	Infection	0.00273291246481375	LHGDN
4137	MAPT	C0001957	Alcohol Withdrawal Delirium	0.00273291246481375	LHGDN
4137	MAPT	C0006118	Brain Neoplasms	0.00273291246481375	LHGDN
4137	MAPT	C0043121	Wernicke Encephalopathy	0.00273291246481375	LHGDN
4137	MAPT	C0442874	Neuropathy	0.0026817553075011	BEFREE;GAD
4137	MAPT	C0006111	Brain Diseases	0.0026817553075011	BEFREE;GAD
4137	MAPT	C0700095	Central neuroblastoma	0.0024725410579179	BEFREE
4137	MAPT	C1270972	Mild cognitive disorder	0.0024725410579179	BEFREE
4137	MAPT	C0027819	Neuroblastoma	0.0024725410579179	BEFREE
4137	MAPT	C1140680	Malignant neoplasm of ovary	0.002407028523288	GAD
4137	MAPT	C0004153	Atherosclerosis	0.002407028523288	GAD
4137	MAPT	C0004352	Autistic Disorder	0.002407028523288	GAD
4137	MAPT	C0007282	Carotid Stenosis	0.002407028523288	GAD
4137	MAPT	C0007786	Brain Ischemia	0.002407028523288	GAD
4137	MAPT	C0011570	Mental Depression	0.002407028523288	GAD
4137	MAPT	C0013421	Dystonia	0.002407028523288	GAD
4137	MAPT	C0021943	Chromosome inversion	0.002407028523288	GAD
4137	MAPT	C0023418	leukemia	0.002407028523288	GAD
4137	MAPT	C0029121	Oppositional Defiant Disorder	0.002407028523288	GAD
4137	MAPT	C0033922	Psychomotor Disorders	0.002407028523288	GAD
4137	MAPT	C0040053	Thrombosis	0.002407028523288	GAD
4137	MAPT	C0041671	Attention Deficit Disorder	0.002407028523288	GAD
4137	MAPT	C0149654	Conduct Disorder	0.002407028523288	GAD
4137	MAPT	C0338460	Argyrophilic grain disease	0.0021978142737048	BEFREE
4137	MAPT	C0006142	Malignant neoplasm of breast	0.0021978142737048	BEFREE
4137	MAPT	C0678222	Breast Carcinoma	0.0019230874894917	BEFREE
4137	MAPT	C0752347	Lewy Body Disease	0.0016483607052786	BEFREE
4137	MAPT	C0494463	Alzheimer Disease, Late Onset	0.0013736339210655	BEFREE
4137	MAPT	C0235946	Cerebral atrophy	0.0013736339210655	BEFREE
4137	MAPT	C0020179	Huntington Disease	0.0010989071368524	BEFREE
4137	MAPT	C0027126	Myotonic Dystrophy	0.0010989071368524	BEFREE
4137	MAPT	C0027765	nervous system disorder	0.0010989071368524	BEFREE
4137	MAPT	C0233514	Abnormal behavior	0.0010989071368524	BEFREE
4137	MAPT	C0276496	Familial Alzheimer Disease (FAD)	0.0008241803526393	BEFREE
4137	MAPT	C0424295	Hyperactive behavior	0.0008241803526393	BEFREE
4137	MAPT	C0520716	Pallidopontonigral degeneration	0.0008241803526393	BEFREE
4137	MAPT	C0750901	Alzheimer Disease, Early Onset	0.0008241803526393	BEFREE
4137	MAPT	C1852467	Creutzfeldt-Jakob Disease, Sporadic	0.0008241803526393	BEFREE
4137	MAPT	C1868193	PNEUMOTHORAX, PRIMARY SPONTANEOUS	0.0008241803526393	BEFREE
4137	MAPT	C0002622	Amnesia	0.0008241803526393	BEFREE
4137	MAPT	C0085084	Motor Neuron Disease	0.0008241803526393	BEFREE
4137	MAPT	C0270736	Essential Tremor	0.0005494535684262	BEFREE
4137	MAPT	C0270920	Supranuclear paralysis	0.0005494535684262	BEFREE
4137	MAPT	C0278488	Carcinoma breast stage IV	0.0005494535684262	BEFREE
4137	MAPT	C0349204	Nonorganic psychosis	0.0005494535684262	BEFREE
4137	MAPT	C0424605	Developmental delay (disorder)	0.0005494535684262	BEFREE
4137	MAPT	C0426980	Motor symptoms	0.0005494535684262	BEFREE
4137	MAPT	C0521175	Neuropil Threads	0.0005494535684262	BEFREE
4137	MAPT	C0524528	Pervasive Development Disorder	0.0005494535684262	BEFREE
4137	MAPT	C0557874	Global developmental delay	0.0005494535684262	BEFREE
4137	MAPT	C0677886	Epithelial ovarian cancer	0.0005494535684262	BEFREE
4137	MAPT	C0751265	Learning Disabilities	0.0005494535684262	BEFREE
4137	MAPT	C0751713	Inclusion Body Myopathy, Sporadic	0.0005494535684262	BEFREE
4137	MAPT	C1458155	Mammary Neoplasms	0.0005494535684262	BEFREE
4137	MAPT	C2750737	DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL	0.0005494535684262	BEFREE
4137	MAPT	C3714756	Intellectual Disability	0.0005494535684262	BEFREE
4137	MAPT	C0008497	Choriocarcinoma	0.0005494535684262	BEFREE
4137	MAPT	C0011989	Camurati-Engelmann Syndrome	0.0005494535684262	BEFREE
4137	MAPT	C0033975	Psychotic Disorders	0.0005494535684262	BEFREE
4137	MAPT	C0220756	Niemann-Pick Disease, Type C	0.0005494535684262	BEFREE
4137	MAPT	C0238190	Inclusion Body Myositis (disorder)	0.0002747267842131	BEFREE
4137	MAPT	C0264611	Apraxia of Phonation	0.0002747267842131	BEFREE
4137	MAPT	C0266617	Congenital anomaly of face	0.0002747267842131	BEFREE
4137	MAPT	C0332996	Persistent embryonic structure	0.0002747267842131	BEFREE
4137	MAPT	C0349081	Dementia in Parkinson's disease	0.0002747267842131	BEFREE
4137	MAPT	C0520789	Progressive subcortical gliosis	0.0002747267842131	BEFREE
4137	MAPT	C0525041	Neurobehavioral Manifestations	0.0002747267842131	BEFREE
4137	MAPT	C0553604	Myotonic Disorders	0.0002747267842131	BEFREE
4137	MAPT	C0564567	Impulsive character (finding)	0.0002747267842131	BEFREE
4137	MAPT	C0595905	cortex bone disorders	0.0002747267842131	BEFREE
4137	MAPT	C0600104	Obsessive compulsive behavior	0.0002747267842131	BEFREE
4137	MAPT	C0699791	Stomach Carcinoma	0.0002747267842131	BEFREE
4137	MAPT	C0700635	Strudwick syndrome	0.0002747267842131	BEFREE
4137	MAPT	C0740279	Atrophy of cerebellum	0.0002747267842131	BEFREE
4137	MAPT	C0751071	Familial Dementia	0.0002747267842131	BEFREE
4137	MAPT	C0751421	Hemispatial Neglect	0.0002747267842131	BEFREE
4137	MAPT	C0751783	Lafora Disease	0.0002747267842131	BEFREE
4137	MAPT	C0871189	Psychotic symptom	0.0002747267842131	BEFREE
4137	MAPT	C0917796	Optic Atrophy, Hereditary, Leber	0.0002747267842131	BEFREE
4137	MAPT	C1112261	Gaze palsy	0.0002747267842131	BEFREE
4137	MAPT	C1258666	Myxoid cyst	0.0002747267842131	BEFREE
4137	MAPT	C1261473	Sarcoma	0.0002747267842131	BEFREE
4137	MAPT	C1262091	Lymphocytic infiltration	0.0002747267842131	BEFREE
4137	MAPT	C1285162	Degenerative disorder	0.0002747267842131	BEFREE
4137	MAPT	C1392786	Cognitive changes	0.0002747267842131	BEFREE
4137	MAPT	C1838313	Pick Complex	0.0002747267842131	BEFREE
4137	MAPT	C1839259	Bulbo-Spinal Atrophy, X-Linked	0.0002747267842131	BEFREE
4137	MAPT	C1853926	NONAKA MYOPATHY	0.0002747267842131	BEFREE
4137	MAPT	C1862941	Amyotrophic Lateral Sclerosis, Sporadic	0.0002747267842131	BEFREE
4137	MAPT	C2220255	Motor disturbances	0.0002747267842131	BEFREE
4137	MAPT	C2718001	Protein Misfolding Disorders	0.0002747267842131	BEFREE
4137	MAPT	C2732618	Sessile Serrated Adenoma/Polyp	0.0002747267842131	BEFREE
4137	MAPT	C2900450	Other Creutzfeldt-Jakob disease	0.0002747267842131	BEFREE
4137	MAPT	C2931822	Nasopharyngeal carcinoma	0.0002747267842131	BEFREE
4137	MAPT	C3273225	Hereditary Neurodegenerative Disorder	0.0002747267842131	BEFREE
4137	MAPT	C3711381	Hereditary Diffuse Leukoencephalopathy with Spheroids	0.0002747267842131	BEFREE
4137	MAPT	C3899989	Autosomal Dominant Disorder	0.0002747267842131	BEFREE
4137	MAPT	C4024896	Motor neuron atrophy	0.0002747267842131	BEFREE
4137	MAPT	C0001614	Adrenal Cortex Diseases	0.0002747267842131	BEFREE
4137	MAPT	C0003550	Broca Aphasia	0.0002747267842131	BEFREE
4137	MAPT	C0007222	Cardiovascular Diseases	0.0002747267842131	BEFREE
4137	MAPT	C0011253	Delusions	0.0002747267842131	BEFREE
4137	MAPT	C0011268	Senile dementia	0.0002747267842131	BEFREE
4137	MAPT	C0011847	Diabetes	0.0002747267842131	BEFREE
4137	MAPT	C0011849	Diabetes Mellitus	0.0002747267842131	BEFREE
4137	MAPT	C0014544	Epilepsy	0.0002747267842131	BEFREE
4137	MAPT	C0015393	Eye Abnormalities	0.0002747267842131	BEFREE
4137	MAPT	C0017495	Gerstmann-Straussler-Scheinker Disease	0.0002747267842131	BEFREE
4137	MAPT	C0018524	Hallucinations	0.0002747267842131	BEFREE
4137	MAPT	C0019348	Herpes Simplex Infections	0.0002747267842131	BEFREE
4137	MAPT	C0023449	Acute lymphocytic leukemia	0.0002747267842131	BEFREE
4137	MAPT	C0024623	Malignant neoplasm of stomach	0.0002747267842131	BEFREE
4137	MAPT	C0025362	Mental Retardation	0.0002747267842131	BEFREE
4137	MAPT	C0026848	Myopathy	0.0002747267842131	BEFREE
4137	MAPT	C0027066	Myoclonus	0.0002747267842131	BEFREE
4137	MAPT	C0027121	Myositis	0.0002747267842131	BEFREE
4137	MAPT	C0027627	Neoplasm Metastasis	0.0002747267842131	BEFREE
4137	MAPT	C0029925	Ovarian Carcinoma	0.0002747267842131	BEFREE
4137	MAPT	C0030193	Pain	0.0002747267842131	BEFREE
4137	MAPT	C0031941	Pineal Gland Neoplasm	0.0002747267842131	BEFREE
4137	MAPT	C0032580	Adenomatous Polyposis Coli	0.0002747267842131	BEFREE
4137	MAPT	C0036572	Seizures	0.0002747267842131	BEFREE
4137	MAPT	C0037019	Shy-Drager Syndrome	0.0002747267842131	BEFREE
4137	MAPT	C0042769	Virus Diseases	0.0002747267842131	BEFREE
4137	MAPT	C0085648	Synovial Cyst	0.0002747267842131	BEFREE
4137	MAPT	C0154671	Degenerative brain disorder	0.0002747267842131	BEFREE
4137	MAPT	C0221505	Lesion of brain	0.0002747267842131	BEFREE
4137	MAPT	C0234213	Sensory denervation disorder	0.0002747267842131	BEFREE