Term Name: | pontocerebellar hypoplasia type 1E |
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Synonyms: | PCH1E |
Definition: | A pontocerebellar hypoplasia type 1 characterized by onset shortly after birth of severe hypotonia and respiratory insufficiency with most patients dying within weeks of birth that has_material_basis_in homozygous or compound heterozygous mutation in the SLC25A46 gene on chromosome 5q22.1. |
Ontology: | Human Disease [DOID:0112330] ( DOID:0112330 ) |