World Of Taxonomy
C157266Level 9

Left Ventricular Noncompaction 7

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant sub-type of left ventricular noncompaction syndrome caused by heterozygous mutation(s) of the MIB1 gene, encoding E3 ubiquitin-protein ligase MIB1.

**Synonyms:** - LVNC7

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