Pontocerebellar hypoplasia, type 11
MONDO:0054669Also known as: PCH11, Pontocerebellar hypoplasia due to TBC1D23, pontocerebellar hypoplasia, type 11
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)