syndromic disease congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome https://www.malacards.org/card/congenital_brachyesophagus_intrathoracic_stomach_vertebral_anomalies_syndrome GARD:0022076 UMLS:C5680208 serpentine-like syndrome MEDGEN:1807957 MONDO:0034895 Orphanet:514352 A rare syndromic esophageal malformation characterized by severe congenital brachyesophagus with midline diaphragmatic hernia and secondary intrathoracic stomach, and vertebral anomalies (in particular rachischisis of the cervical/thoracic spine). Additional reported manifestations include intrauterine growth restriction, short neck, intestinal malrotation, herniation of other abdominal organs, and cleft lip, among others. The condition is mostly fatal in the neonatal or early infantile period.