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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
4744	NEFH	C0002736	Amyotrophic Lateral Sclerosis	0.409037273124398	BEFREE;HPO;LHGDN;ORPHANET
4744	NEFH	C0524851	Neurodegenerative Disorders	0.20328236603324	BEFREE;HPO;LHGDN
4744	NEFH	C0003467	Anxiety	0.2	HPO
4744	NEFH	C0011581	Depressive disorder	0.2	HPO
4744	NEFH	C0013404	Dyspnea	0.2	HPO
4744	NEFH	C0015672	Fatigue	0.2	HPO
4744	NEFH	C0026821	Muscle Cramp	0.2	HPO
4744	NEFH	C0026838	Muscle Spasticity	0.2	HPO
4744	NEFH	C0027746	Nerve Degeneration	0.2	HPO
4744	NEFH	C0030193	Pain	0.2	HPO
4744	NEFH	C0031117	Peripheral Neuropathy	0.2	CTD_human
4744	NEFH	C0043352	Xerostomia	0.2	HPO
4744	NEFH	C0085633	Mood swings	0.2	HPO
4744	NEFH	C0234958	muscle degeneration	0.2	HPO
4744	NEFH	C0270948	Neurogenic Muscular Atrophy	0.2	HPO
4744	NEFH	C0522224	Paralysed	0.2	HPO
4744	NEFH	C0541794	Skeletal muscle atrophy	0.2	HPO
4744	NEFH	C0746674	Generalized muscle weakness	0.2	HPO
4744	NEFH	C1145670	Respiratory Failure	0.2	HPO
4744	NEFH	C1843479	Neurogenic muscle atrophy, especially in the lower limbs	0.2	HPO
4744	NEFH	C1862939	AMYOTROPHIC LATERAL SCLEROSIS 1	0.2	CTD_human
4744	NEFH	C4020854	Neuro-degenerative disease	0.2	HPO
4744	NEFH	C4020884	Anxiety disease	0.2	HPO
4744	NEFH	C4022587	Fatigable weakness of respiratory muscles	0.2	HPO
4744	NEFH	C4022588	Fatigable weakness of swallowing muscles	0.2	HPO
4744	NEFH	C0007787	Transient Ischemic Attack	0.08	RGD
4744	NEFH	C0010308	Congenital Hypothyroidism	0.08	RGD
4744	NEFH	C0011853	Diabetes Mellitus, Experimental	0.08	RGD
4744	NEFH	C0020676	Hypothyroidism	0.08	RGD
4744	NEFH	C0031485	Phenylketonurias	0.08	RGD
4744	NEFH	C0043020	Wallerian Degeneration	0.08	RGD
4744	NEFH	C0149940	Sciatic Neuropathy	0.08	RGD
4744	NEFH	C0085084	Motor Neuron Disease	0.00864587664824215	BEFREE;GAD;LHGDN
4744	NEFH	C0036341	Schizophrenia	0.002407028523288	GAD
4744	NEFH	C0029925	Ovarian Carcinoma	0.0010989071368524	BEFREE
4744	NEFH	C1140680	Malignant neoplasm of ovary	0.0010989071368524	BEFREE
4744	NEFH	C0027832	Neurofibromatosis 2	0.0008241803526393	BEFREE
4744	NEFH	C0020538	Hypertensive disease	0.0005494535684262	BEFREE
4744	NEFH	C3887505	DYSFUNCTION - SKIN DISORDERS	0.0005494535684262	BEFREE
4744	NEFH	C4024896	Motor neuron atrophy	0.0005494535684262	BEFREE
4744	NEFH	C0002395	Alzheimer's Disease	0.0002747267842131	BEFREE
4744	NEFH	C0006142	Malignant neoplasm of breast	0.0002747267842131	BEFREE
4744	NEFH	C0007134	Renal Cell Carcinoma	0.0002747267842131	BEFREE
4744	NEFH	C0010823	Cytomegalovirus Infections	0.0002747267842131	BEFREE
4744	NEFH	C0013080	Down Syndrome	0.0002747267842131	BEFREE
4744	NEFH	C0027765	nervous system disorder	0.0002747267842131	BEFREE
4744	NEFH	C0027819	Neuroblastoma	0.0002747267842131	BEFREE
4744	NEFH	C0028754	Obesity	0.0002747267842131	BEFREE
4744	NEFH	C0085580	Essential Hypertension	0.0002747267842131	BEFREE
4744	NEFH	C0178874	Tumor Progression	0.0002747267842131	BEFREE
4744	NEFH	C0234133	Extrapyramidal sign	0.0002747267842131	BEFREE
4744	NEFH	C0236642	Pick Disease of the Brain	0.0002747267842131	BEFREE
4744	NEFH	C0262395	borderline hypertension	0.0002747267842131	BEFREE
4744	NEFH	C0279626	Squamous cell carcinoma of esophagus	0.0002747267842131	BEFREE
4744	NEFH	C0338451	Frontotemporal dementia	0.0002747267842131	BEFREE
4744	NEFH	C0600139	Prostate carcinoma	0.0002747267842131	BEFREE
4744	NEFH	C0677886	Epithelial ovarian cancer	0.0002747267842131	BEFREE
4744	NEFH	C0678222	Breast Carcinoma	0.0002747267842131	BEFREE
4744	NEFH	C0700095	Central neuroblastoma	0.0002747267842131	BEFREE
4744	NEFH	C1839259	Bulbo-Spinal Atrophy, X-Linked	0.0002747267842131	BEFREE
4744	NEFH	C2239176	Liver carcinoma	0.0002747267842131	BEFREE