Term Name:	pontocerebellar hypoplasia type 10
Synonyms:
Definition:	A pontocerebellar hypoplasia that is characterized by severe developmental delays, progressive microcephaly, spasticity and seizure, has_material_basis_in autosomal recessive inheritance of mutation in the CLP1 gene.
Ontology:	Human Disease [DOID:0060279]   ( DOID:0060279 )