Monarch Disease Ontology identifier MONDO_0010494 (linear skin defects with multiple congenital anomalies 3) is any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the NDUFB11 gene. Also known as: NDUFB11 microphthalmia with linear skin defects syndrome, linear skin defects with multiple congenital anomalies 3, X-linked dominant, linear skin defects with multiple congenital anomalies type 3, microphthalmia with linear skin defects syndrome caused by mutation in NDUFB11.