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

GeneID Gene_Symbol DisGeNet_diseaseID Disease_name DisGeNet score DisGeNet_sourceDB
1062CENPEC0265202Seckel syndrome0.200274726784213BEFREE;ORPHANET
1062CENPEC1400105Hypertrophy of nose0.2HPO
1062CENPEC0431368Partial agenesis of corpus callosum0.2HPO
1062CENPEC4020876Dull intelligence0.2HPO
1062CENPEC4015080MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE0.2UNIPROT
1062CENPEC0541764Delayed bone age0.2HPO
1062CENPEC4012968Mild global developmental delay0.2HPO
1062CENPEC0575802Small hand0.2HPO
1062CENPEC3714756Intellectual Disability0.2HPO
1062CENPEC3553764Joint hyperflexibility0.2HPO
1062CENPEC0683322Mental impairment0.2HPO
1062CENPEC2749675Cortical gyral simplification0.2HPO
1062CENPEC0917816Mental deficiency0.2HPO
1062CENPEC2229182Psychomotor retardation, mild0.2HPO
1062CENPEC1386048Intrauterine retardation0.2HPO
1062CENPEC0424688Small head0.2HPO
1062CENPEC1865037Cone-shaped epiphyses0.2HPO
1062CENPEC1837463Narrow face0.2HPO
1062CENPEC1840069Sandal gap0.2HPO
1062CENPEC1843367Poor school performance0.2HPO
1062CENPEC1848673Hypoplastic feet0.2HPO
1062CENPEC1849121Thin face0.2HPO
1062CENPEC1849364Absent earlobe0.2HPO
1062CENPEC1850049Bilateral fifth finger clinodactyly0.2HPO
1062CENPEC1856468Round, full face0.2HPO
1062CENPEC1857042Sparse scalp hair0.2HPO
1062CENPEC1857130Hypoplastic mandible condyle0.2HPO
1062CENPEC1857278Partial or complete agenesis of corpus callosum0.2HPO
1062CENPEC1857656Precociously senile appearance0.2HPO
1062CENPEC1857679Sloping forehead0.2HPO
1062CENPEC4024202Reduced number of teeth0.2HPO
1062CENPEC4280629Hyperplasia of nose0.2HPO
1062CENPEC0006625Cachexia0.2HPO
1062CENPEC4280615Defective tooth enamel0.2HPO
1062CENPEC0010278Craniosynostosis0.2HPO
1062CENPEC0014544Epilepsy0.2HPO
1062CENPEC0015934Fetal Growth Retardation0.2HPO
1062CENPEC0017601Glaucoma0.2HPO
1062CENPEC0019555Hip Dislocation, Congenital0.2HPO
1062CENPEC0021296Infant, Small for Gestational Age0.2HPO
1062CENPEC4280538Curvature of little finger0.2HPO
1062CENPEC0025362Mental Retardation0.2HPO
1062CENPEC0025990Micrognathism0.2HPO
1062CENPEC4280262Dystrophic tooth enamel0.2HPO
1062CENPEC4083050Agenesis of teeth0.2HPO
1062CENPEC0426415Large nose0.2HPO
1062CENPEC0036572Seizures0.2HPO
1062CENPEC0235942Skull malformation0.2HPO
1062CENPEC0239479Round face0.2HPO
1062CENPEC0240295Mandibular hypoplasia0.2HPO
1062CENPEC0240538Convex nasal ridge0.2HPO
1062CENPEC0266470Cerebellar Hypoplasia0.2HPO
1062CENPEC0338656Impaired cognition0.2HPO
1062CENPEC4021800Enamel abnormalities0.2HPO
1062CENPEC0349588Short stature0.2HPO
1062CENPEC0423110Downward slant of palpebral fissure0.2HPO
1062CENPEC0423903Low intelligence0.2HPO
1062CENPEC4020899Autosomal recessive predisposition0.2HPO
1062CENPEC0006142Malignant neoplasm of breast0.0026817553075011BEFREE;GAD
1062CENPEC0001973Alcoholic Intoxication, Chronic0.002407028523288GAD
1062CENPEC0700095Central neuroblastoma0.0005494535684262BEFREE
1062CENPEC0027819Neuroblastoma0.0005494535684262BEFREE
1062CENPEC0432246Microcephalic Osteodysplastic Primordial Dwarfism, Type II0.0002747267842131BEFREE
1062CENPEC0009402Colorectal Carcinoma0.0002747267842131BEFREE
1062CENPEC0025202melanoma0.0002747267842131BEFREE
1062CENPEC0032002Pituitary Diseases0.0002747267842131BEFREE
1062CENPEC0036421Systemic Scleroderma0.0002747267842131BEFREE
1062CENPEC0346153Breast Cancer, Familial0.0002747267842131BEFREE
1062CENPEC0424605Developmental delay (disorder)0.0002747267842131BEFREE
1062CENPEC1527249Colorectal Cancer0.0002747267842131BEFREE
1062CENPEC0521158Recurrent tumor0.0002747267842131BEFREE
1062CENPEC0557874Global developmental delay0.0002747267842131BEFREE
1062CENPEC0596263Carcinogenesis0.0002747267842131BEFREE
1062CENPEC0678222Breast Carcinoma0.0002747267842131BEFREE
1062CENPEC3539878Triple Negative Breast Neoplasms0.0002747267842131BEFREE
1062CENPEC2239176Liver carcinoma0.0002747267842131BEFREE
1062CENPEC1292778Chronic myeloproliferative disorder0.0002747267842131BEFREE