striatonigral degeneration
| UniProt ID | Protein Name | Source |
|---|---|---|
| P37198 | Nuclear pore glycoprotein p62 |
| HPO ID | HPO Term |
|---|---|
| HP:0002020 | Gastroesophageal reflux |
| HP:0007688 | Undetectable light- and dark-adapted electroretinogram |
| HP:0001276 | Hypertonia |
| HP:0002446 | Astrocytosis |
| HP:0001256 | Intellectual disability, mild |
| HP:0006799 | Basal ganglia cysts |
| HP:0001336 | Myoclonus |
| HP:0012758 | Neurodevelopmental delay |
| HP:0002273 | Tetraparesis |
| HP:0000750 | Delayed speech and language development |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 4, 2025