striatonigral degeneration
| UniProt ID | Protein Name | Source |
|---|---|---|
| P37198 | Nuclear pore glycoprotein p62 |
| HPO ID | HPO Term |
|---|---|
| HP:0000648 | Optic atrophy |
| HP:0000750 | Delayed speech and language development |
| HP:0001251 | Ataxia |
| HP:0001256 | Intellectual disability, mild |
| HP:0001257 | Spasticity |
| HP:0001260 | Dysarthria |
| HP:0001266 | Choreoathetosis |
| HP:0001276 | Hypertonia |
| HP:0001285 | Spastic tetraparesis |
| HP:0001288 | Gait disturbance |
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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: April 6, 2026