Pontocerebellar hypoplasia, type 15
MONDO:0030259Also known as: PCH15, pontocerebellar hypoplasia, type 15
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)