Pontocerebellar hypoplasia, type 1F
MONDO:0030261Also known as: PCH1F, pontocerebellar hypoplasia, type 1F
1 clinical trial for this condition and its sub-types.
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Disease
(680)
Nervous system disorder
(231)
Hereditary disease
(176)
Human disease
(14)
Developmental defect during embryogenesis
(8)
Hereditary neurological disease
(6)
Central nervous system malformation
(5)
Disease of genetic or genomic mechanism
(2)
Pontocerebellar hypoplasia
(1)
Disease by body system or component
(0)