Human genes for Kleefstra syndrome 2
Kleefstra syndrome 2 [DOID:0080598]
A Kleefstra syndrome that is characterized by delayed psychomotor development, variable intellectual disability, and mild dysmorphic features and has_material_basis_in heterozygous mutation in the KMT2C gene on chromosome 7q36.
Synonyms: Kleefstra syndrome 2, DOID:0080598