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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 |
|---|---|---|---|---|---|
| C0017185 | Gastrointestinal Neoplasms | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0205696 | Anaplastic carcinoma | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0019348 | Herpes Simplex Infections | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C1864100 | PSEUDOHYPOPARATHYROIDISM, TYPE IB | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0085084 | Motor Neuron Disease | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C1851584 | Childhood Ependymoma | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0023521 | Globoid cell leukodystrophy | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0037822 | Speech Disorders | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0032285 | Pneumonia | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0158981 | Neonatal diabetes mellitus | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0004903 | Beckwith-Wiedemann Syndrome | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C1458155 | Mammary Neoplasms | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0558356 | Malignant melanoma of eye | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0014474 | Ependymoma | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0029456 | Osteoporosis | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0007113 | Rectal Carcinoma | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0699790 | Colon Carcinoma | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0020456 | Hyperglycemia | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0002395 | Alzheimer's Disease | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| C0041408 | Turner Syndrome | ASAH1 | 427 | N-acylsphingosine amidohydrolase 1 | Q13510 |
| 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 |
