* We recommend a score >= 0.08 for meaningful Gene-Disease associations
GeneID | Gene_Symbol | DisGeNet_diseaseID | Disease_name | DisGeNet score | DisGeNet_sourceDB |
10087 | COL4A3BP | C1847514 | Postnatal microcephaly | 0.2 | HPO |
10087 | COL4A3BP | C0494475 | Tonic - clonic seizures | 0.2 | HPO |
10087 | COL4A3BP | C0558165 | Curly hair (finding) | 0.2 | HPO |
10087 | COL4A3BP | C0678230 | Congenital Epicanthus | 0.2 | HPO |
10087 | COL4A3BP | C0856863 | Broad-based gait | 0.2 | HPO |
10087 | COL4A3BP | C0917816 | Mental deficiency | 0.2 | HPO |
10087 | COL4A3BP | C1142533 | Smooth philtrum | 0.2 | HPO |
10087 | COL4A3BP | C1384666 | hearing impairment | 0.2 | HPO |
10087 | COL4A3BP | C1827524 | Wide spaced nipples | 0.2 | HPO |
10087 | COL4A3BP | C1840077 | Anteverted nostril | 0.2 | HPO |
10087 | COL4A3BP | C1843367 | Poor school performance | 0.2 | HPO |
10087 | COL4A3BP | C1844813 | Widely spaced teeth | 0.2 | HPO |
10087 | COL4A3BP | C0557874 | Global developmental delay | 0.2 | HPO |
10087 | COL4A3BP | C1848673 | Hypoplastic feet | 0.2 | HPO |
10087 | COL4A3BP | C1853743 | Axial hypotonia | 0.2 | HPO |
10087 | COL4A3BP | C1864897 | Cognitive delay | 0.2 | HPO |
10087 | COL4A3BP | C1865916 | Bilateral ptosis | 0.2 | HPO |
10087 | COL4A3BP | C3550658 | Maternal oligohydramnios | 0.2 | HPO |
10087 | COL4A3BP | C3714756 | Intellectual Disability | 0.2 | HPO |
10087 | COL4A3BP | C4020875 | Mental and motor retardation | 0.2 | HPO |
10087 | COL4A3BP | C4020876 | Dull intelligence | 0.2 | HPO |
10087 | COL4A3BP | C4048268 | Cortical visual impairment | 0.2 | HPO |
10087 | COL4A3BP | C4072834 | Rough hair texture | 0.2 | HPO |
10087 | COL4A3BP | C4225156 | MENTAL RETARDATION, AUTOSOMAL DOMINANT 34 | 0.2 | UNIPROT |
10087 | COL4A3BP | C0431447 | Synophrys | 0.2 | HPO |
10087 | COL4A3BP | C0006325 | Bruxism | 0.2 | HPO |
10087 | COL4A3BP | C0007131 | Non-Small Cell Lung Carcinoma | 0.2 | CTD_human |
10087 | COL4A3BP | C0011053 | Deafness | 0.2 | HPO |
10087 | COL4A3BP | C0013132 | Drooling | 0.2 | HPO |
10087 | COL4A3BP | C0018772 | Hearing Loss, Partial | 0.2 | HPO |
10087 | COL4A3BP | C0025362 | Mental Retardation | 0.2 | HPO |
10087 | COL4A3BP | C0037036 | Sialorrhea | 0.2 | HPO |
10087 | COL4A3BP | C0038271 | Stereotyped Behavior | 0.2 | HPO |
10087 | COL4A3BP | C0038273 | Stereotypic Movement Disorder | 0.2 | HPO |
10087 | COL4A3BP | C0079924 | Oligohydramnios | 0.2 | HPO |
10087 | COL4A3BP | C0155320 | Blindness, Cortical | 0.2 | HPO |
10087 | COL4A3BP | C0332615 | Myopathic facies | 0.2 | HPO |
10087 | COL4A3BP | C0277959 | Coarse hair | 0.2 | HPO |
10087 | COL4A3BP | C0339789 | Congenital deafness | 0.2 | HPO |
10087 | COL4A3BP | C0432040 | Simple syndactyly of toes, first web space | 0.2 | HPO |
10087 | COL4A3BP | C0423109 | Upward slant of palpebral fissure | 0.2 | HPO |
10087 | COL4A3BP | C0423903 | Low intelligence | 0.2 | HPO |
10087 | COL4A3BP | C0006142 | Malignant neoplasm of breast | 0.0005494535684262 | BEFREE |
10087 | COL4A3BP | C0678222 | Breast Carcinoma | 0.0005494535684262 | BEFREE |
10087 | COL4A3BP | C0004364 | Autoimmune Diseases | 0.0002747267842131 | BEFREE |
10087 | COL4A3BP | C0002395 | Alzheimer's Disease | 0.0002747267842131 | BEFREE |
10087 | COL4A3BP | C0017658 | Glomerulonephritis | 0.0002747267842131 | BEFREE |
10087 | COL4A3BP | C3539878 | Triple Negative Breast Neoplasms | 0.0002747267842131 | BEFREE |
10087 | COL4A3BP | C2936349 | Plaque, Amyloid | 0.0002747267842131 | BEFREE |
10087 | COL4A3BP | C0403529 | Anti-Glomerular Basement Membrane Disease | 0.0002747267842131 | BEFREE |
10087 | COL4A3BP | C0029925 | Ovarian Carcinoma | 0.0002747267842131 | BEFREE |
10087 | COL4A3BP | C1140680 | Malignant neoplasm of ovary | 0.0002747267842131 | BEFREE |
10087 | COL4A3BP | C0333463 | Senile Plaques | 0.0002747267842131 | BEFREE |