has material basis in autosomal dominant disease oocyte/zygote/embryo maturation arrest oocyte/zygote/embryo maturation arrest 3 ORDO:404466 ORDO:404466 disease_ontology MIM:617712 An oocyte/zygote/embryo maturation arrest that is characterized by infertility, caused by absence of the zona pellucida that results in degeneration of oocytes and 'empty follicle syndrome' on in vitro fertilization procedures and that has_material_basis_in heterozygous mutation in the ZP3 gene on chromosome 7q11.23. UMLS_CUI:C4749433 DOID:0061305 OOMD3 OZEMA3 UMLS_CUI:C4749433 female infertility due to zona pellucida defect. oocyte maturation defect 3 autosomal dominant inheritance