Chiari type I malformation, Corneal dystrophy, Corneal opacity, Cortical pulverulent cataract, Delayed cranial suture closure, Depressed nasal bridge, Developmental cataract, Downslanted palpebral fissures, Facial asymmetry, Flat face, Hearing impairment, High forehead, Hypertelorism, Intellectual disability, Iris coloboma, Long philtrum, Low-set ears, Macular hypoplasia, Malar flattening, Mandibular prognathia, Microcornea, Microtia, Midface retrusion, Myopia, Nail dystrophy, Narrow mouth, Nuclear cataract, Nystagmus, Pectus excavatum, Pericarditis, Photophobia, Posteriorly rotated ears, Ptosis, Radioulnar synostosis, Retinal detachment, Seizure, Sensorineural hearing impairment, Short nose, Short stature, Smooth philtrum, Sparse scalp hair, Tapered finger, Thin upper lip vermilion, Upslanted palpebral fissure, Visual impairment, Wide nasal bridge

abnormal placenta morphology, abnormal placenta vasculature, abnormal prepulse inhibition, abnormal pupillary reflex, abnormal startle reflex, abnormal tail morphology, abnormal umbilical cord morphology, decreased body size, decreased freezing behavior, decreased interleukin-4 secretion, decreased pacinian corpuscle number, decreased prepulse inhibition, dilated renal tubules, embryonic lethality during organogenesis, incomplete penetrance, increased lymphoma incidence, increased plasma cell number, increased startle reflex, lethality throughout fetal growth and development, incomplete penetrance, neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, renal cast, small liver, small pacinian corpuscles, small pupils, tubular nephritis, vision/eye phenotype, weakness