Linear skin defects with multiple congenital anomalies 3

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, 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, LSDMCA3, linear skin defects with cardiomyopathy and Other congenital anomalies

16 clinical trials for this condition and its sub-types.