Term Name:	neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies
Synonyms:	autosomal recessive mental retardation 36
Definition:	An autosomal recessive intellectual developmental disorder that is characterized by global developmental delay with delayed walking, impaired intellectual development, and speech delay apparent from infancy or early childhood and that has_material_basis_in homozygous mutation in the ADAT3 gene on chromosome 19p13.
Ontology:	Human Disease [DOID:0081099]   ( DOID:0081099 )