DO_rare_slim has material basis in autosomal recessive disease congenital diarrhea microvillus inclusion disease ICD10CM:P78.3 disease_ontology GARD:7039 MESH:C537470 A congenital diarrhea characterized by onset of intractable life-threatening watery diarrhea during infancy, lack of microvilli on the surface of enterocytes and occurrence of intracellular vacuolar structures containing microvilli that has_material_basis_in homozygous or compound heterozygous mutation in the MYO5B gene on chromosome 18q21. DOID:0060775 Davidson disease MIM:251850 MVD ORDO:2290 congenital familial protracted diarrhea with enterocyte brush-border abnormalities congenital microvillus atrophy diarrhea 2 with microvillus atrophy intractable diarrhea of infancy autosomal recessive inheritance