has material basis in germline mutation in RBM10 TARP syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/10089/tarp-syndrome https://www.malacards.org/card/tarp_syndrome talipes equinovarus - atrial septal defect - Robin sequence - persistence of the left superior vena cava Pierre Robin syndrome with congenital heart malformation and clubfoot GARD:0010089 Pierre Robin syndrome-congenital heart defect-talipes syndrome UMLS:C1839463 SCTID:725911008 A rare developmental defect during embryogenesis syndrome characterized by Robin sequence (micrognathia, glossoptosis, and cleft palate), atrial septal defect, persistence of the left superior vena cava, and talipes equinovarus. The phenotype is variable, some patients present with further dysmorphic characteristics (e.g. hypertelorism, ear abnormalities) while others do not have any key findings. Additional features, such as syndactyly, polydactyly, or brain anomalies (e.g. cerebellar hypoplasia), have also been reported. The syndrome is almost invariably lethal with affected males either dying prenatally or living just a few months. talipes equinovarus-atrial septal defect-Robin sequence-persistence of the left superior vena cava syndrome Pierre Robin sequence - congenital heart defect - talipes TARP syndrome, X-linked recessive MEDGEN:333324 DOID:0111780 Pierre Robin syndrome - congenital heart defect - talipes MONDO:0010711 Pierre Robin sequence-congenital heart defect-talipes syndrome OMIM:311900 tarp syndrome TARPS Orphanet:2886 MESH:C536942 talipes equinovarus, atrial septal defect, Robin sequence, and persistence of left Superior vena cava obsolete syndrome or malformation associated with head and neck malformations cardiogenetic disease