Antley-Bixler syndrome SNOMEDCT_US_2020_03_01:62964007 OMIM:207410 disease_ontology OMIM:201750 A syndrome that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene. DOID:0050462 OMIM mapping confirmed by DO. [SN]. MESH:D054882 trapezoidocephaly-synostosis syndrome autosomal recessive disease syndrome