linear skin defects with multiple congenital anomalies 3 (DOID:0111876)
Alliance: disease page
Synonyms: linear skin defects with cardiomyopathy and other congenital anomalies; LSDMCA3
Alt IDs: OMIM:300952
Definition: A linear skin defects with multiple congenital anomalies characterized by linear skin defects, cardiomyopathy, and various other congenital anomalies that has_material_basis_in heterozygous mutation in the NDUFB11 gene on chromosome Xp11.3.