DO_rare_slim has material basis in autosomal recessive disease fetal encasement syndrome A syndrome that has_material_basis_in homozygous mutation in the CHUK gene on chromosome 10q24 and is characterized by multiple fetal malformations including defective face and seemingly absent limbs, which are bound to the trunk and encased under the skin. ORDO:465824 DOID:0060647 cocoon syndrome disease_ontology MIM:613630 syndrome autosomal recessive inheritance