Human genes for Waisman syndrome
Waisman syndrome [DOID:0111781]
A syndrome characterized by delayed psychomotor development, impaired intellectual development, and early-onset Parkinson disease that has_material_basis_in hemizygous or homozygous mutation in RAB39B on chromosome Xq28.
Synonyms: Waisman syndrome, DOID:0111781, Waisman disease, Waisman disorder, Waisman syndromes ...