Human genes for GAND syndrome
GAND syndrome [DOID:0070048]
An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay apparent from infancy, with motor delay and moderate to severely impaired intellectual development and that has_material_basis_in an autosomal dominant mutation of GATAD2B on chromosome 1q21.3.
Synonyms: GAND syndrome, DOID:0070048, GAND disease, GAND disorder, GAND syndromes ...