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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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SUBCORTICAL GLIOSIS OF NEUMANN
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C5561929 |
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leukoencephalopathy, diffuse hereditary, with spheroids 1
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C5561929 |
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Subcortical gliosis of Neumann
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C5561929 |
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Pigmentary orthochromatic leukodystrophy
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C5561929 |
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pigmentary orthochromatic leukodystrophy
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C5561929 |
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hereditary diffuse leukoencephalopathy with axonal spheroids
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C5561929 |
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CSF1R-related adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
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C5561929 |
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Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia
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C5561929 |
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Autosomal dominant leukoencephalopathy with neuroaxonal spheroids
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C5561929 |
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autosomal dominant leukoencephalopathy with neuroaxonal spheroids
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C5561929 |
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Hereditary diffuse leukoencephalopathy with spheroids
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C5561929 |
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leukoencephalopathy with neuroaxonal spheroids, autosomal dominant
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C5561929 |
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subcortical gliosis of Neumann
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C5561929 |
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Gliosis, familial progressive subcortical
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C5561929 |
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gliosis, familial progressive subcortical
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C5561929 |
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