Pontocerebellar hypoplasia, type 16
MONDO:0030438Also known as: PCH16
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)