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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
27247	NFU1	C3276432	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1	0.4	ORPHANET;UNIPROT
27247	NFU1	C0001125	Acidosis, Lactic	0.2	HPO
27247	NFU1	C0020542	Pulmonary Hypertension	0.2	HPO
27247	NFU1	C0023380	Lethargy	0.2	HPO
27247	NFU1	C0151786	Muscle Weakness	0.2	HPO
27247	NFU1	C0231246	Failure to gain weight	0.2	HPO
27247	NFU1	C0232466	Feeding difficulties	0.2	HPO
27247	NFU1	C0347959	Lactic acidemia	0.2	HPO
27247	NFU1	C0557874	Global developmental delay	0.2	HPO
27247	NFU1	C1145670	Respiratory Failure	0.2	HPO
27247	NFU1	C1835995	Decreased activities of mitochondrial-encoded respiratory chain complexes	0.2	HPO
27247	NFU1	C1864897	Cognitive delay	0.2	HPO
27247	NFU1	C2315100	Pediatric failure to thrive	0.2	HPO
27247	NFU1	C2973725	Pulmonary arterial hypertension	0.2	HPO
27247	NFU1	C3203102	Idiopathic pulmonary arterial hypertension	0.2	HPO
27247	NFU1	C3276441	Decreased activity of mitochondrial respiratory complexes	0.2	HPO
27247	NFU1	C4020875	Mental and motor retardation	0.2	HPO
27247	NFU1	C4020899	Autosomal recessive predisposition	0.2	HPO
27247	NFU1	C4024609	Decreased activity of mitochondrial respiratory chain	0.2	HPO
27247	NFU1	C0006111	Brain Diseases	0.0008241803526393	BEFREE
27247	NFU1	C0085584	Encephalopathies	0.0008241803526393	BEFREE
27247	NFU1	C0270612	Leukoencephalopathies	0.0005494535684262	BEFREE
27247	NFU1	C0026848	Myopathy	0.0002747267842131	BEFREE
27247	NFU1	C0037772	Spastic Paraplegia	0.0002747267842131	BEFREE
27247	NFU1	C0162670	Mitochondrial Myopathies	0.0002747267842131	BEFREE
27247	NFU1	C0268559	Hyperglycinemia	0.0002747267842131	BEFREE
27247	NFU1	C0747251	Progressive spastic paraparesis	0.0002747267842131	BEFREE
27247	NFU1	C0751651	Mitochondrial Diseases	0.0002747267842131	BEFREE
27247	NFU1	C0751783	Lafora Disease	0.0002747267842131	BEFREE