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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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ANOAC
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C5680002 |
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Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome
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C5680002 |
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Axonal neuropathy-optic atrophy-cognitive deficit syndrome
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C5680002 |
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axonal neuropathy-optic atrophy-cognitive deficit syndrome
|
C5680002 |
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Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome
|
C5680002 |
|
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infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome
|
C5680002 |
|
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ANOAC (axonal neuropathy, optic atrophy, cognitive deficit) syndrome
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C5680002 |
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Axonal neuropathy, optic atrophy, cognitive deficit syndrome
|
C5680002 |
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