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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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Hereditary spastic paraplegia 9A
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C5568978 |
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hereditary spastic paraplegia 9A
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C5568978 |
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hereditary spastic paraplegia type 9A
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C5568978 |
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Spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome
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C5568978 |
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Autosomal dominant spastic paraparesis
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C5568978 |
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autosomal dominant spastic paraplegia 9A
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C5568978 |
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Autosomal dominant spastic paraplegia type 9A
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C5568978 |
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Cataracts-motor neuropathy-short stature-skeletal anomalies syndrome
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C5568978 |
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spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux
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C5568978 |
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spastic paraparesis with amyopathy, cataracts, and gastroesophageal reflux
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C5568978 |
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spastic paraparesis with amyotrophy, cataracts, and gastroesophageal reflux
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C5568978 |
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