* We recommend a score >= 0.08 for meaningful Gene-Disease associations
GeneID | Gene_Symbol | DisGeNet_diseaseID | Disease_name | ![]() | DisGeNet_sourceDB |
1062 | CENPE | C0265202 | Seckel syndrome | 0.200274726784213 | BEFREE;ORPHANET |
1062 | CENPE | C1400105 | Hypertrophy of nose | 0.2 | HPO |
1062 | CENPE | C0431368 | Partial agenesis of corpus callosum | 0.2 | HPO |
1062 | CENPE | C4020876 | Dull intelligence | 0.2 | HPO |
1062 | CENPE | C4015080 | MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE | 0.2 | UNIPROT |
1062 | CENPE | C0541764 | Delayed bone age | 0.2 | HPO |
1062 | CENPE | C4012968 | Mild global developmental delay | 0.2 | HPO |
1062 | CENPE | C0575802 | Small hand | 0.2 | HPO |
1062 | CENPE | C3714756 | Intellectual Disability | 0.2 | HPO |
1062 | CENPE | C3553764 | Joint hyperflexibility | 0.2 | HPO |
1062 | CENPE | C0683322 | Mental impairment | 0.2 | HPO |
1062 | CENPE | C2749675 | Cortical gyral simplification | 0.2 | HPO |
1062 | CENPE | C0917816 | Mental deficiency | 0.2 | HPO |
1062 | CENPE | C2229182 | Psychomotor retardation, mild | 0.2 | HPO |
1062 | CENPE | C1386048 | Intrauterine retardation | 0.2 | HPO |
1062 | CENPE | C0424688 | Small head | 0.2 | HPO |
1062 | CENPE | C1865037 | Cone-shaped epiphyses | 0.2 | HPO |
1062 | CENPE | C1837463 | Narrow face | 0.2 | HPO |
1062 | CENPE | C1840069 | Sandal gap | 0.2 | HPO |
1062 | CENPE | C1843367 | Poor school performance | 0.2 | HPO |
1062 | CENPE | C1848673 | Hypoplastic feet | 0.2 | HPO |
1062 | CENPE | C1849121 | Thin face | 0.2 | HPO |
1062 | CENPE | C1849364 | Absent earlobe | 0.2 | HPO |
1062 | CENPE | C1850049 | Bilateral fifth finger clinodactyly | 0.2 | HPO |
1062 | CENPE | C1856468 | Round, full face | 0.2 | HPO |
1062 | CENPE | C1857042 | Sparse scalp hair | 0.2 | HPO |
1062 | CENPE | C1857130 | Hypoplastic mandible condyle | 0.2 | HPO |
1062 | CENPE | C1857278 | Partial or complete agenesis of corpus callosum | 0.2 | HPO |
1062 | CENPE | C1857656 | Precociously senile appearance | 0.2 | HPO |
1062 | CENPE | C1857679 | Sloping forehead | 0.2 | HPO |
1062 | CENPE | C4024202 | Reduced number of teeth | 0.2 | HPO |
1062 | CENPE | C4280629 | Hyperplasia of nose | 0.2 | HPO |
1062 | CENPE | C0006625 | Cachexia | 0.2 | HPO |
1062 | CENPE | C4280615 | Defective tooth enamel | 0.2 | HPO |
1062 | CENPE | C0010278 | Craniosynostosis | 0.2 | HPO |
1062 | CENPE | C0014544 | Epilepsy | 0.2 | HPO |
1062 | CENPE | C0015934 | Fetal Growth Retardation | 0.2 | HPO |
1062 | CENPE | C0017601 | Glaucoma | 0.2 | HPO |
1062 | CENPE | C0019555 | Hip Dislocation, Congenital | 0.2 | HPO |
1062 | CENPE | C0021296 | Infant, Small for Gestational Age | 0.2 | HPO |
1062 | CENPE | C4280538 | Curvature of little finger | 0.2 | HPO |
1062 | CENPE | C0025362 | Mental Retardation | 0.2 | HPO |
1062 | CENPE | C0025990 | Micrognathism | 0.2 | HPO |
1062 | CENPE | C4280262 | Dystrophic tooth enamel | 0.2 | HPO |
1062 | CENPE | C4083050 | Agenesis of teeth | 0.2 | HPO |
1062 | CENPE | C0426415 | Large nose | 0.2 | HPO |
1062 | CENPE | C0036572 | Seizures | 0.2 | HPO |
1062 | CENPE | C0235942 | Skull malformation | 0.2 | HPO |
1062 | CENPE | C0239479 | Round face | 0.2 | HPO |
1062 | CENPE | C0240295 | Mandibular hypoplasia | 0.2 | HPO |
1062 | CENPE | C0240538 | Convex nasal ridge | 0.2 | HPO |
1062 | CENPE | C0266470 | Cerebellar Hypoplasia | 0.2 | HPO |
1062 | CENPE | C0338656 | Impaired cognition | 0.2 | HPO |
1062 | CENPE | C4021800 | Enamel abnormalities | 0.2 | HPO |
1062 | CENPE | C0349588 | Short stature | 0.2 | HPO |
1062 | CENPE | C0423110 | Downward slant of palpebral fissure | 0.2 | HPO |
1062 | CENPE | C0423903 | Low intelligence | 0.2 | HPO |
1062 | CENPE | C4020899 | Autosomal recessive predisposition | 0.2 | HPO |
1062 | CENPE | C0006142 | Malignant neoplasm of breast | 0.0026817553075011 | BEFREE;GAD |
1062 | CENPE | C0001973 | Alcoholic Intoxication, Chronic | 0.002407028523288 | GAD |
1062 | CENPE | C0700095 | Central neuroblastoma | 0.0005494535684262 | BEFREE |
1062 | CENPE | C0027819 | Neuroblastoma | 0.0005494535684262 | BEFREE |
1062 | CENPE | C0432246 | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | 0.0002747267842131 | BEFREE |
1062 | CENPE | C0009402 | Colorectal Carcinoma | 0.0002747267842131 | BEFREE |
1062 | CENPE | C0025202 | melanoma | 0.0002747267842131 | BEFREE |
1062 | CENPE | C0032002 | Pituitary Diseases | 0.0002747267842131 | BEFREE |
1062 | CENPE | C0036421 | Systemic Scleroderma | 0.0002747267842131 | BEFREE |
1062 | CENPE | C0346153 | Breast Cancer, Familial | 0.0002747267842131 | BEFREE |
1062 | CENPE | C0424605 | Developmental delay (disorder) | 0.0002747267842131 | BEFREE |
1062 | CENPE | C1527249 | Colorectal Cancer | 0.0002747267842131 | BEFREE |
1062 | CENPE | C0521158 | Recurrent tumor | 0.0002747267842131 | BEFREE |
1062 | CENPE | C0557874 | Global developmental delay | 0.0002747267842131 | BEFREE |
1062 | CENPE | C0596263 | Carcinogenesis | 0.0002747267842131 | BEFREE |
1062 | CENPE | C0678222 | Breast Carcinoma | 0.0002747267842131 | BEFREE |
1062 | CENPE | C3539878 | Triple Negative Breast Neoplasms | 0.0002747267842131 | BEFREE |
1062 | CENPE | C2239176 | Liver carcinoma | 0.0002747267842131 | BEFREE |
1062 | CENPE | C1292778 | Chronic myeloproliferative disorder | 0.0002747267842131 | BEFREE |