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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
1069	CETN2	C0043346	Xeroderma Pigmentosum	0.00273291246481375	LHGDN
1069	CETN2	C0006142	Malignant neoplasm of breast	0.002407028523288	GAD
1069	CETN2	C0004114	Astrocytoma	0.0002747267842131	BEFREE
1069	CETN2	C0020255	Hydrocephalus	0.0002747267842131	BEFREE
1069	CETN2	C0025286	Meningioma	0.0002747267842131	BEFREE
1069	CETN2	C0032019	Pituitary Neoplasms	0.0002747267842131	BEFREE
1069	CETN2	C0035335	Retinoblastoma	0.0002747267842131	BEFREE
1069	CETN2	C0162429	Malnutrition	0.0002747267842131	BEFREE
1069	CETN2	C0235287	Dysosmia	0.0002747267842131	BEFREE
1069	CETN2	C0278488	Carcinoma breast stage IV	0.0002747267842131	BEFREE
1069	CETN2	C1762616	Meningioma, benign, no ICD-O subtype	0.0002747267842131	BEFREE
1069	CETN2	C2752147	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C	0.0002747267842131	BEFREE
1069	CETN2	C3888024	Cacosmia	0.0002747267842131	BEFREE
1069	CETN2	C4277690	Ciliopathies	0.0002747267842131	BEFREE