Term Name:	intellectual disability-severe speech delay-mild dysmorphism syndrome
Synonyms:	FOXP1 Haploinsufficiency, FOXP1 syndrome, FOXP1-Related Neurodevelopmental Disorder, Mental retardation with language impairment and with or without autistic features
Definition:	A syndromic intellectual disability characterized by global developmental delay with moderate to severe speech delay, dysmorphic craniofacial features, and gross motor skill delays that particularly affects expressive speech that has_material_basis_in heterozygous mutation in the FOXP1 gene on chromosome 3p13.
Ontology:	Human Disease [DOID:0111331]   ( DOID:0111331 )