/linear skin defects with multiple congenital anomalies 3
linear skin defects with multiple congenital anomalies 3
Rare Disease
MONDO:0010494
Also Known As
NDUFB11 microphthalmia with linear skin defects syndromelinear skin defects with multiple congenital anomalies 3linear skin defects with multiple congenital anomalies 3, X-linked dominantlinear skin defects with multiple congenital anomalies type 3microphthalmia with linear skin defects syndrome caused by mutation in NDUFB11LSDMCA3linear skin defects with cardiomyopathy and Other congenital anomalies
Definition
Any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the NDUFB11 gene.
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