Human genes for Birk-Barel syndrome
Birk-Barel syndrome [DOID:0050675]
A syndrome that is characterized by intellectual disability, hypotonia, hyperactivity and facies, has_material_basis_in heterozygous mutation in the KCNK9 gene on chromosome 8q24.
Synonyms: Birk-Barel syndrome, BirkBarel syndrome, Birk-Barel disease, Birk-Barel disorder, Birk-Barel syndromes ...
Linkouts: OMIM