Term Name: | pontocerebellar hypoplasia type 14 |
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Synonyms: | PCH14 |
Definition: | A pontocerebellar hypoplasia characterized by congenital onset of progressive microcephaly, poor or absent psychomotor development, and severely impaired intellectual development that has_material_basis_in homozygous or compound heterozygous mutation in the PPIL1 gene on chromosome 6p21.2. |
Ontology: | Human Disease [DOID:0112325] ( DOID:0112325 ) |