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Hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome

MONDO:0018655

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (717) Nervous system disorder (243) Hereditary disease (188) Neurodegenerative disease (182) Central nervous system disorder (115) Human disease (15) Inherited neurodegenerative disorder (10) Hereditary neurological disease (6) Leukodystrophy (5) Disease of genetic or genomic mechanism (2)

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