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| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
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ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
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C1859598 |
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Ataxia, Adult-Onset, With Oculomotor Apraxia
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C1859598 |
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Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia
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C1859598 |
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APTX oculomotor apraxia or related oculomotor disease
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C1859598 |
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Ataxia oculomotor apraxia type 1
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C1859598 |
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Early-onset cerebellar ataxia with hypoalbuminemia
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C1859598 |
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early-onset cerebellar ataxia with hypoalbuminemia
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C1859598 |
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Adult onset ataxia with oculomotor apraxia
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C1859598 |
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Autosomal recessive ataxia with oculomotor apraxia type 1
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C1859598 |
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Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
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C1859598 |
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cerebellar ataxia, early-onset, with hypoalbuminemia
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C1859598 |
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ataxia with oculomotor apraxia type 1
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C1859598 |
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AOA1 (ataxia oculomotor apraxia type 1)
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C1859598 |
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oculomotor apraxia or related oculomotor disease caused by mutation in APTX
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C1859598 |
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Ataxia-oculomotor apraxia syndrome
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C1859598 |
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