1 results
Disease Disease Group: monogenic disease Genes: Foxp2 (Mmu)
Source: DOID:0111275
Definition: A speech disorder characterized by severe orofacial dyspraxia resulting in largely incomprehensible speech that has_material_basis_in heterozygous mutation in FOXP2 on 7q31.1.
Genes: Foxp2 (Mmu)