Term Name:	neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that is characterized by the onset of features in infancy or early childhood and that has_material_basis_in homozygous or compound heterozygous mutation in the INTS11 gene on chromosome 1p36.
Ontology:	Human Disease [DOID:0081387]   ( DOID:0081387 )