obsolete_Lopes-Maciel-Rodan syndrome true MONDO:0054573 Replaced by Mondo term MONDO_0054573, with which this term was previously merged. Use: http://purl.obolibrary.org/obo/MONDO_0054573 OMIM:617435 An autosomal recessive neurodevelopmental disorder characterized by developmental regression in infancy, delayed psychomotor development, severe intellectual disability, and cerebral and cerebellar atrophy. Additional features include swallowing problems, dystonia, bradykinesia, and continuous manual stereotypies without chorea. Some patients manifest seizures. 3.88.0 https://www.uniprot.org/diseases/DI-04988 http://purl.obolibrary.org/obo/MONDO_0054573 LOMARS