Leukoencephalopathy with vanishing white matter 1
MONDO:0020507Any leukoencephalopathy with vanishing white matter in which the cause of the disease is a variation in the EIF2B1 gene.
Also known as: CACH, childhood ataxia with central nervous system hypomyelinization, vanishing white matter leukodystrophy, Cree leukoencephalopathy
19 clinical trials for this condition and its sub-types.
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Disease
(618)
Nervous system disorder
(217)
Hereditary disease
(172)
Neurodegenerative disease
(155)
Central nervous system disorder
(97)
Human disease
(14)
Inherited neurodegenerative disorder
(10)
Leukoencephalopathy with vanishing white matter
(7)
Hereditary neurological disease
(5)
Leukodystrophy
(5)