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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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C3711381 |
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GPSC
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C3711381 |
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HDLS
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C3711381 |
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POLD
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C3711381 |
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Neuroaxonal Leukodystrophy
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C3711381 |
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DEMENTIA, FAMILIAL, NEUMANN TYPE
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C3711381 |
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Pigmentary Orthochromatic Leukodystrophy
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C3711381 |
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Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
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C3711381 |
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Autosomal Dominant Leukoencephalopathy with Neuroaxonal Spheroids
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C3711381 |
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Hereditary Diffuse Leukoencephalopathy with Spheroids
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C3711381 |
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LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS
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C3711381 |
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Leukoencephalopathy, Diffuse Hereditary, With Spheroids
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C3711381 |
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LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT
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C3711381 |
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GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL
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C3711381 |
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Dementia, Familial, Neumann Type
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C3711381 |
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