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Metadata
ID	DOID:0060279
Name	pontocerebellar hypoplasia type 10
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. https://www.omim.org/entry/615803
Xrefs	OMIM:615803 ORDO:411493
Subsets	DO_rare_slim
Parent Relationships	is_a pontocerebellar hypoplasia