L-2-hydroxyglutaric aciduria
| HPO ID | HPO Term |
|---|---|
| HP:0002062 | Abnormal pyramidal tract morphology |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0002171 | Gliosis |
| HP:0001251 | Ataxia |
| HP:0000639 | Nystagmus |
| HP:0007256 | Abnormal pyramidal sign |
| HP:0000365 | Hearing impairment |
| HP:0002352 | Leukoencephalopathy |
| HP:0001272 | Cerebellar atrophy |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026