Pontocerebellar hypoplasia, type 12
MONDO:0032643Also known as: COASY-related pontocerebellar hypoplasia, PCH12, PONTOCEREBELLAR HYPOPLASIA, TYPE 12
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)