neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies (DOID:0081099)
Alliance: disease page
Synonyms: autosomal recessive mental retardation 36
Alt IDs: OMIM:615286
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.