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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 |
|---|---|---|---|---|---|
| C0002170 | Alopecia | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0028738 | Nystagmus | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0524851 | Neurodegenerative Disorders | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0700095 | Central neuroblastoma | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C2677586 | Spastic Paraplegia 39, Autosomal Recessive | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0027819 | Neuroblastoma | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0027765 | nervous system disorder | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0037773 | Spastic Paraplegia, Hereditary | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0154681 | Anterior Horn Cell Disease | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C1848745 | Oliver-McFarlane syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0442874 | Neuropathy | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0011882 | Diabetic Neuropathies | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C3714756 | Intellectual Disability | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0020758 | Congenital ichthyosis | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0020757 | Ichthyoses | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0271683 | Polyneuropathy, Motor | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0917799 | Hypersomnia | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0270763 | Familial Motor Neuron Disease | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0009714 | Hepatic Fibrosis, Congenital | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0085084 | Motor Neuron Disease | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0011570 | Mental Depression | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0037050 | Sick Building Syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C1854520 | SEBASTIAN SYNDROME | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0022735 | Klinefelter Syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
