"ORDO:86818"^^ . "SNOMEDCT_US_2021_09_01:720982007"^^ . . _:vb50945620 . _:vb50945620 _:vb50945617 . _:vb50945618 . "AMME complex"^^ . _:vb50945616 . "OMIM:300194"^^ . "DOID:0111860"^^ . _:vb50945620 _:vb50945619 . _:vb50945618 . _:vb50945619 _:vb50945618 . _:vb50945617 . _:vb50945616 . _:vb50945619 . _:vb50945617 . _:vb50945617 . _:vb50945616 _:vb50945620 . "A syndrome characterized by Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis that has_material_basis_in hemizygous deletion of multiple genes including COL4A5, FACL4 and AMMECR1 on chromosome Xq22.3."^^ . "Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome"^^ . "disease_ontology"^^ . "chromosome Xq22.3 telomeric deletion syndrome"^^ . _:vb50945616 . _:vb50945617 . "MESH:C564570"^^ . "AMME syndrome"^^ . _:vb50945619 . "ATS-MR"^^ . _:vb50945618 . . "UMLS_CUI:C1846242"^^ . . _:vb50945618 . .