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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 |
|---|---|---|---|---|---|
| C0006826 | Malignant Neoplasms | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0014070 | Encephalomyelitis | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0011849 | Diabetes Mellitus | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C1306459 | Primary malignant neoplasm | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0023890 | Liver Cirrhosis | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0013421 | Dystonia | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C1621958 | Glioblastoma Multiforme | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0008055 | Chikungunya Fever | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0003873 | Rheumatoid Arthritis | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0011847 | Diabetes | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0022658 | Kidney Diseases | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0012236 | DiGeorge Syndrome | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C1306759 | Eosinophilic disorder | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0751495 | Seizures, Focal | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C3179349 | Gastrointestinal Stromal Sarcoma | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
| C0006142 | Malignant neoplasm of breast | ASAH2B | 653308 | N-acylsphingosine amidohydrolase 2B | P0C7U1 |
| C0678222 | Breast Carcinoma | ASAH2B | 653308 | N-acylsphingosine amidohydrolase 2B | P0C7U1 |
| C0011849 | Diabetes Mellitus | ASAH2 | 56624 | N-acylsphingosine amidohydrolase 2 | Q9NR71 |
| C0018852 | Heavy Chain Disease | ASAH2 | 56624 | N-acylsphingosine amidohydrolase 2 | Q9NR71 |
| C0235833 | Congenital diaphragmatic hernia | ASAH2 | 56624 | N-acylsphingosine amidohydrolase 2 | Q9NR71 |
| C0010674 | Cystic Fibrosis | ASAH2 | 56624 | N-acylsphingosine amidohydrolase 2 | Q9NR71 |
| C0018854 | gamma-Chain Disease | ASAH2 | 56624 | N-acylsphingosine amidohydrolase 2 | Q9NR71 |
| C0023895 | Liver diseases | ASAH2 | 56624 | N-acylsphingosine amidohydrolase 2 | Q9NR71 |
| C0700095 | Central neuroblastoma | ASAH2 | 56624 | N-acylsphingosine amidohydrolase 2 | Q9NR71 |
| C0017601 | Glaucoma | ASAH2 | 56624 | N-acylsphingosine amidohydrolase 2 | Q9NR71 |
