DO_rare_slim has material basis in existence starts during autosomal recessive disease neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome A syndrome that is characterized in infants showing respiratory insufficiency and almost no spontaneous movement at birth, usually requiring mechanical ventilation and admission to the neonatal intensive care unit and that has_material_basis_in compound heterozygous mutation in the ATAD3A gene on chromosome 1p36.33. ORDO:615983 disease_ontology MIM:618810 DOID:0081396 PHRINL syndrome syndrome autosomal recessive inheritance Neonatal onset