X-linked complicated spastic paraplegia type 1
MONDO:0017630An X-linked form of L1 syndrome characterized by spastic paraplegia, mild to moderate intellectual disability, normal MRI of the brain.
Also known as: SPG1
0 clinical trials for this condition and its sub-types.
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Disease
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Hereditary disease
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X-linked disease
(16)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
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Disorder of development or morphogenesis
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L1 syndrome
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X-linked recessive disease
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