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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 |
|---|---|---|---|---|---|
| C0280324 | Laryngeal Squamous Cell Carcinoma | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C0024623 | Malignant neoplasm of stomach | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C0585442 | Osteosarcoma of bone | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C0008707 | Chronic osteomyelitis | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C0699791 | Stomach Carcinoma | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C0740457 | Malignant neoplasm of kidney | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C0684249 | Carcinoma of lung | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C0017661 | IGA Glomerulonephritis | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C1306459 | Primary malignant neoplasm | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C0345904 | Malignant neoplasm of liver | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C0685938 | Malignant neoplasm of gastrointestinal tract | ACYP2 | 98 | acylphosphatase 2 | P14621 |
| C0003493 | Aortic Diseases | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0003507 | Aortic Valve Stenosis | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0432269 | Lenz Majewski hyperostotic dwarfism | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C1851710 | LATERAL MENINGOCELE SYNDROME | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0036439 | Scoliosis, unspecified | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0010495 | Cutis Laxa | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0039075 | Syndactyly | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0015934 | Fetal Growth Retardation | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0008297 | Choanal Atresia | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0004352 | Autistic Disorder | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C3714756 | Intellectual Disability | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0013336 | Dwarfism | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0019294 | Hernia, Inguinal | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0015469 | Facial paralysis | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
