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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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AR-SPG9B
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C5568980 |
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SPG9B
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C5568980 |
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autosomal recessive complex spastic paraplegia caused by mutation in ALDH18A1
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C5568980 |
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SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE
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C5568980 |
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spastic paraplegia 9B, autosomal recessive
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C5568980 |
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Spastic paraplegia 9b, autosomal recessive
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C5568980 |
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Autosomal recessive complex spastic paraplegia type 9B
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C5568980 |
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autosomal recessive complex spastic paraplegia type 9B
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C5568980 |
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ALDH18A1 autosomal recessive complex spastic paraplegia
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C5568980 |
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hereditary spastic paraplegia 9B
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C5568980 |
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autosomal recessive spastic paraplegia 9B
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C5568980 |
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Autosomal recessive spastic paraplegia type 9B
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C5568980 |
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hereditary spastic paraplegia type 9B
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C5568980 |
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