left ventricular noncompaction 7
Findings
No curated finding names left ventricular noncompaction 7 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any left ventricular noncompaction in which the cause of the disease is a mutation in the MIB1 gene.
Definition from the Mondo Disease Ontology (MONDO:0014042), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
2 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Left ventricular noncompactionHPOHP:0030682
- Left ventricular noncompaction cardiomyopathyHPOHP:0011664
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- MIB1HGNC:21086
- Moderate · PanelApp Australia · Autosomal dominant · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2017
Where it sits
- A kind of
Other names
3 names
Resolves to: left ventricular noncompaction 7
- Also called
- left ventricular noncompaction caused by mutation in MIB1left ventricular noncompaction type 7MIB1 left ventricular noncompaction