autosomal recessive intellectual developmental disorder 11 (DOID:0081186)
Alliance: disease page
Alt IDs: OMIM:611097
Definition: An autosomal recessive intellectual developmental disorder that has_material_basis_in a candidate locus on chromosome 19q, termed MRT11. Haplotype analysis delineated a 5.4-Mb candidate region between SNPs rs2109075 and rs8101149.