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Here is the list of developmental anomalies associated with this developmental anomaly, based on the cases' information :

• Right bilobate lung 5.19% (4/77 anomalies), in cases MDB49, MDB215, MDB435, MDB518
• Facial dysmorphism 5.19% (4/77 anomalies), in cases MDB202, MDB215, MDB518, MDB5
• Placenta hypoplasia 2.6% (2/77 anomalies), in cases MDB49, MDB215
• Pulmonary hypoplasia 2.6% (2/77 anomalies), in cases MDB202, MDB518
• Cleft palate, median posterior 2.6% (2/77 anomalies), in cases MDB215, MDB518
• Low-set ears 2.6% (2/77 anomalies), in cases MDB215, MDB518
• Talipes equinovarus, bilateral 2.6% (2/77 anomalies), in cases MDB215, MDB5
• Syndactyly of the feet , simple (webbed), unilateral 1.3% (1/77 anomalies), in case MDB49
• Syndactyly of the toes, unilateral 1.3% (1/77 anomalies), in case MDB49
• Adrenal hypoplasia, fetal 1.3% (1/77 anomalies), in case MDB49
• Syndactyly, simple (webbed), fingers 1.3% (1/77 anomalies), in case MDB49
• Macrocephaly 1.3% (1/77 anomalies), in case MDB202
• Frontal bossing 1.3% (1/77 anomalies), in case MDB202
• Microtia 1.3% (1/77 anomalies), in case MDB202
• Prominent and pointed nose 1.3% (1/77 anomalies), in case MDB202
• Hydrocephalus 1.3% (1/77 anomalies), in case MDB202
• Congenitally Corrected Transposition of the Great Arteries 1.3% (1/77 anomalies), in case MDB202
• Interauricular communication 1.3% (1/77 anomalies), in case MDB202
• Dandy-Walker malformation 1.3% (1/77 anomalies), in case MDB202
• Micromelia 1.3% (1/77 anomalies), in case MDB215
• Microphthalmia 1.3% (1/77 anomalies), in case MDB215
• Hypertelorism 1.3% (1/77 anomalies), in case MDB215
• Broad nasal bridge 1.3% (1/77 anomalies), in case MDB215
• Short neck 1.3% (1/77 anomalies), in case MDB215
• Clindodactyly of 5th finger, bilateral 1.3% (1/77 anomalies), in case MDB215
• Multicystic renal dysplasia,bilateral 1.3% (1/77 anomalies), in case MDB215
• Intrauterine growth retardation, symmetric 1.3% (1/77 anomalies), in case MDB215
• Single umblical artery (SUA)-Isolated 1.3% (1/77 anomalies), in case MDB215
• Dextroposition of aorta 1.3% (1/77 anomalies), in case MDB435
• overlapping skull bones 1.3% (1/77 anomalies), in case MDB435
• Lumbosacral agenesis 1.3% (1/77 anomalies), in case MDB518
• Relative Macrocephaly 1.3% (1/77 anomalies), in case MDB518
• Narrow thorax 1.3% (1/77 anomalies), in case MDB518
• Long philtrum 1.3% (1/77 anomalies), in case MDB518
• Retrognathia 1.3% (1/77 anomalies), in case MDB518
• Overlapping fingers 1.3% (1/77 anomalies), in case MDB518
• Clindodactyly of 5th finger, unilateral 1.3% (1/77 anomalies), in case MDB518
• Renal agenesis, bilateral 1.3% (1/77 anomalies), in case MDB518
• Agenesia of internal genital organs 1.3% (1/77 anomalies), in case MDB518
• Thymic hypoplasia 1.3% (1/77 anomalies), in case MDB518
• Persistent truncus arteriosus 1.3% (1/77 anomalies), in case MDB518
• Right aortic arch 1.3% (1/77 anomalies), in case MDB518
• Gastroschisis 1.3% (1/77 anomalies), in case MDB518
• Rachischisis 1.3% (1/77 anomalies), in case MDB518
• Vertebral hypoplasia, dorsolumbar 1.3% (1/77 anomalies), in case MDB518
• Rib deformation with abnormal numbers, bilateral 1.3% (1/77 anomalies), in case MDB518
• Underdeveloped pelvic bones 1.3% (1/77 anomalies), in case MDB518
• Flat face 1.3% (1/77 anomalies), in case MDB5
• Flattened occiput 1.3% (1/77 anomalies), in case MDB5
• Epicanthus 1.3% (1/77 anomalies), in case MDB5
• Macroglossia 1.3% (1/77 anomalies), in case MDB5
• Transverse palmar crease, bilateral 1.3% (1/77 anomalies), in case MDB5
• Atrial Hypertrophy 1.3% (1/77 anomalies), in case MDB5
• Overlapping toes 1.3% (1/77 anomalies), in case MDB5
• Preauricular hamartoma 1.3% (1/77 anomalies), in case MDB5
• Ventricular septal defect, membranous 1.3% (1/77 anomalies), in case MDB5
• Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 1.3% (1/77 anomalies), in case MDB5
• Intestinal malrotation 1.3% (1/77 anomalies), in case MDB5
• Dilatation of ureter , bilateral, congenital 1.3% (1/77 anomalies), in case MDB5
• Fusion of the adrenal glands 1.3% (1/77 anomalies), in case MDB5
• Microsplenia 1.3% (1/77 anomalies), in case MDB5
• Cystic hygroma 1.3% (1/77 anomalies), in case MDB5
• Lung agenesis, unilateral 1.3% (1/77 anomalies), in case MDB5
• Bladder wall thickness 1.3% (1/77 anomalies), in case MDB5
• Amnion nodosum 1.3% (1/77 anomalies), in case MDB5
• Polysplenia 1.3% (1/77 anomalies), in case MDB5