A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability characterized by severe congenital contractures of the limbs and face, hypotonia, neonatal respiratory distress, and global developmental delay. Dysmorphic facial features include downslanting palpebral fissures, broad nasal bridge, large nares, long philtrum, and deep nasolabial folds, among others. Limb deformities (camptodactyly, clubfoot), short neck, scoliosis, as well as seizures have also been reported. Brain MRI may show cerebral and cerebellar atrophy in some cases. The disease is Monarch Disease Ontology identifier MONDO_0014556 (congenital contractures of the limbs and face, hypotonia, and developmental delay). Also known as: CLIFAHDD syndrome, congenital limbs-face contractures-hypotonia-developmental delay syndrome.