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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▲ |
|---|---|---|---|---|---|
| C1842836 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0025958 | Microcephaly | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0005695 | Bladder Neoplasm | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C3714756 | Intellectual Disability | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0038273 | Stereotypic Movement Disorder | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0013384 | Dyskinetic syndrome | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0020490 | Hyperopia | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0005684 | Malignant neoplasm of urinary bladder | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C3280127 | MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0036572 | Seizures | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0282577 | Congenital Disorders of Glycosylation | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0242172 | Pelvic Inflammatory Disease | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C2239176 | Liver carcinoma | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0699885 | Carcinoma of bladder | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0751495 | Seizures, Focal | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0039075 | Syndactyly | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0006826 | Malignant Neoplasms | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0036857 | Severe intellectual disability | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0520947 | Clumsiness - motor delay | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0008489 | Chorea | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0235946 | Cerebral atrophy | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0004352 | Autistic Disorder | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C1868720 | Periventricular Nodular Heterotopia | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C1527366 | Salaam Seizures | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0221757 | alpha 1-Antitrypsin Deficiency | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
