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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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AOA4
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C4225397 |
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oculomotor apraxia or related oculomotor disease caused by mutation in PNKP
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C4225397 |
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ATAXIA-OCULOMOTOR APRAXIA 4
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C4225397 |
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Ataxia-oculomotor apraxia 4
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C4225397 |
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ataxia-oculomotor apraxia 4
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C4225397 |
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PNKP oculomotor apraxia or related oculomotor disease
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C4225397 |
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Ataxia - oculomotor apraxia type 4
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C4225397 |
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ataxia - oculomotor apraxia type 4
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C4225397 |
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ataxia-oculomotor apraxia-4
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C4225397 |
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Ataxia-oculomotor apraxia type 4
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C4225397 |
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