DO_rare_slim has material basis in X-linked monogenic disease TARP syndrome MIM:311900 DOID:0111780 MESH:C536942 ORDO:2886 A syndrome characterized by talipes equinovarus, atrial septal defect, Robin sequence (micrognathia, cleft palate, and glossoptosis), and persistent left superior vena cava typically resulting in late prenatal or early postnatal mortality that has_material_basis_in hemizygous mutation in the RBM10 gene on chromosome Xp11.3. Pierre Robin sequence-congenital heart defect-talipes syndrome Pierre Robin syndrome-congenital heart defect-talipes syndrome UMLS_CUI:C1839463 disease_ontology GARD:10089 SNOMEDCT_US_2025_09_01:725911008 TARPS talipes equinovarus-atrial septal defect-Robin sequence-persistence of the left superior vena cava syndrome syndrome X-linked inheritance