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
GET
/api/v1/systems/nci_thesaurus/nodes/C157266Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.