abnormal kidney development, abnormal kidney mesenchyme morphology, abnormal lens vesicle development, abnormal lower incisor morphology, abnormal mandible morphology, abnormal maxilla morphology, abnormal maxillary shelf morphology, abnormal middle ear ossicle morphology, abnormal nasal capsule morphology, abnormal nasal septum cartilage morphology, abnormal renal glomerulus morphology, abnormal sternocostal joint morphology, abnormal sternum morphology, abnormal temporal bone petrous part morphology, abnormal thyroid cartilage morphology, abnormal vibrissa morphology, abnormal vibrissa number, abnormal xiphoid process morphology, absent cricoid cartilage, absent metanephric mesenchyme, absent thyroid cartilage, absent upper incisors, aphakia, asymmetric sternocostal joints, basisphenoid bone foramen, broad limb buds, cardiovascular system phenotype, decreased body size, decreased erythrocyte cell number, decreased fetal size, decreased molar number, decreased renal glomerulus number, dilated renal glomerular capsule, growth retardation of molars, hair follicle outer root sheath hyperplasia, neonatal lethality, incomplete penetrance, no abnormal phenotype detected, palatal shelf hypoplasia, palatal shelves fail to meet at midline, postnatal lethality, complete penetrance, preweaning lethality, complete penetrance, retina pigment epithelium atrophy, short rostral-caudal axis, skeleton phenotype, small Meckel's cartilage, small basisphenoid bone, small kidney, small pterygoid bone