MedGen Find_IDs Find_Terms Annotation
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created at 2024-09-19 07:43:07 UTC
updated at 2024-09-23 18:19:38 UTC
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
622,528 entries
Label
Id
Leukoencephalopathy, diffuse hereditary, with spheroids 1 C5561929
leukoencephalopathy, diffuse hereditary, with spheroids 1 C5561929
Pigmentary orthochromatic leukodystrophy C5561929
pigmentary orthochromatic leukodystrophy C5561929
hereditary diffuse leukoencephalopathy with axonal spheroids C5561929
CSF1R-related adult-onset leukoencephalopathy with axonal spheroids and pigmented glia C5561929
Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia C5561929
Autosomal dominant leukoencephalopathy with neuroaxonal spheroids C5561929
autosomal dominant leukoencephalopathy with neuroaxonal spheroids C5561929
Hereditary diffuse leukoencephalopathy with spheroids C5561929
leukoencephalopathy with neuroaxonal spheroids, autosomal dominant C5561929
Subcortical gliosis of Neumann C5561929
subcortical gliosis of Neumann C5561929
Gliosis, familial progressive subcortical C5561929
gliosis, familial progressive subcortical C5561929