. . _:vb50941033 . . "DOID:0080493"^^ . "A 46 XX gonadal dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16."^^ . _:vb50941033 . "OMIM:233300"^^ . . "disease_ontology"^^ . "ovarian dysgenesis 1"@en . _:vb50941033 . _:vb50941033 . _:vb50941033 .