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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
54928	IMPAD1	C3279757	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE	0.400274726784213	BEFREE;ORPHANET;UNIPROT
54928	IMPAD1	C0011053	Deafness	0.2	HPO
54928	IMPAD1	C0015300	Exophthalmos	0.2	HPO
54928	IMPAD1	C0018772	Hearing Loss, Partial	0.2	HPO
54928	IMPAD1	C0025990	Micrognathism	0.2	HPO
54928	IMPAD1	C0026034	Microstomia	0.2	HPO
54928	IMPAD1	C0221357	Brachydactyly	0.2	HPO
54928	IMPAD1	C0239676	High forehead	0.2	HPO
54928	IMPAD1	C0240295	Mandibular hypoplasia	0.2	HPO
54928	IMPAD1	C0339789	Congenital deafness	0.2	HPO
54928	IMPAD1	C0349588	Short stature	0.2	HPO
54928	IMPAD1	C0426414	Small nose	0.2	HPO
54928	IMPAD1	C0576093	Knee joint valgus deformity	0.2	HPO
54928	IMPAD1	C1384666	hearing impairment	0.2	HPO
54928	IMPAD1	C1836195	Hypoplastic toes	0.2	HPO
54928	IMPAD1	C1837084	Short metacarpal	0.2	HPO
54928	IMPAD1	C1837760	Prominent eyes	0.2	HPO
54928	IMPAD1	C1839764	Broad flat nasal bridge	0.2	HPO
54928	IMPAD1	C1848490	Protruding eyes	0.2	HPO
54928	IMPAD1	C1848673	Hypoplastic feet	0.2	HPO
54928	IMPAD1	C1849367	Nasal bridge wide	0.2	HPO
54928	IMPAD1	C1853241	Flat face	0.2	HPO
54928	IMPAD1	C1854114	Short nose	0.2	HPO
54928	IMPAD1	C1856266	Coronal craniosynostosis	0.2	HPO
54928	IMPAD1	C1857130	Hypoplastic mandible condyle	0.2	HPO
54928	IMPAD1	C1862425	Prominent globes	0.2	HPO
54928	IMPAD1	C2677762	Tall forehead	0.2	HPO
54928	IMPAD1	C4020899	Autosomal recessive predisposition	0.2	HPO
54928	IMPAD1	C0023418	leukemia	0.0002747267842131	BEFREE
54928	IMPAD1	C0024623	Malignant neoplasm of stomach	0.0002747267842131	BEFREE
54928	IMPAD1	C0038356	Stomach Neoplasms	0.0002747267842131	BEFREE
54928	IMPAD1	C0278701	Gastric Adenocarcinoma	0.0002747267842131	BEFREE
54928	IMPAD1	C0343284	Chondrodysplasia	0.0002747267842131	BEFREE
54928	IMPAD1	C0699791	Stomach Carcinoma	0.0002747267842131	BEFREE