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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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ALSP
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C5561929 |
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FPSG
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C5561929 |
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GPSC
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C5561929 |
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HDLS
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C5561929 |
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HDLS1
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C5561929 |
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POLD
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C5561929 |
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Pigmentary orthochromatic leukodystrophy
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C5561929 |
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CSF1R-related ALSP
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C5561929 |
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neuroaxonal leukodystrophy
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C5561929 |
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Familial dementia, Neumann type
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C5561929 |
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dementia, familial, Neumann type
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C5561929 |
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familial dementia, Neumann type
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C5561929 |
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Leukoencephalopathy, diffuse hereditary, with spheroids 1
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C5561929 |
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leukoencephalopathy, diffuse hereditary, with spheroids 1
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C5561929 |
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LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS 1
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C5561929 |
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