has material basis in disease has basis in Antley-Bixler syndrome with disordered steroidogenesis disease_ontology SNOMEDCT_US_2021_09_01:62964007 DOID:0050462 MIM:201750 MESH:D054882 An Antley-Bixler 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. OMIM mapping confirmed by DO. [SN]. trapezoidocephaly-synostosis syndrome autosomal recessive disease Antley-Bixler syndrome syndrome autosomal recessive inheritance symptom