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DOID:0111876 - linear skin defects with multiple congenital anomalies 3
Disease Ontology 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.
Synonyms: LSDMCA3, linear skin defects with cardiomyopathy and other congenital anomalies,
Xenbase Genes
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Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
MLS syndrome (is_a),
physical disorder (is_a)