Term Name:	neurodevelopmental disorder with eye movement abnormalities and ataxia
Synonyms:	NEDEMA
Definition:	An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay apparent from infancy and that has_material_basis_in heterozygous mutation in the FRMD5 gene on chromosome 15q15. Affected individuals show delayed walking with an unsteady gait, variably impaired intellectual development, learning disabilities, and speech difficulties.
Ontology:	Human Disease [DOID:0081275]   ( DOID:0081275 )