linear skin defects with multiple congenital anomalies 3 Disease Ontology Browser

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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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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