A congenital muscular dystrophy characterized by onset of progressive muscle weakness in early childhood with autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the INPP5K gene (607875) on chromosome 17p13. [ url:https://www.ncbi.nlm.nih.gov/pubmed/28190459 ]. The disease is muscular dystrophy, congenital, with cataracts and intellectual disability (EFO_0009149). Also known as: MDCCAID.