ataxia with oculomotor apraxia type 1 (Q18553452)
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Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal recessive cerebellar ataxia (ARCA; see this term), characterized by progressive cerebellar ataxia associated with oculomotor apraxia, severe neuropathy, and hypoalbuminemia
- AOA1
- ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH
- Ataxia-Telangiectasia-Like Syndrome
- Cerebellar Ataxia, Early-Onset, With Hypoalbuminemia
- Ataxia-oculomotor apraxia type 1
- Ataxia-Oculomotor Apraxia Syndrome
- ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
- EAOH
- Ataxia, Adult-Onset, With Oculomotor Apraxia
- Ataxia-Oculomotor Apraxia 1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | ataxia with oculomotor apraxia type 1 |
Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal recessive cerebellar ataxia (ARCA; see this term), characterized by progressive cerebellar ataxia associated with oculomotor apraxia, severe neuropathy, and hypoalbuminemia |
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