MYH10-related neurodevelopmental disorder with congenital anomalies
MONDO:0700281Mondo
Findings
No curated finding names MYH10-related neurodevelopmental disorder with congenital anomalies yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An autosomal dominant complex neurodevelopmental disorder in which the cause of the disease is a mutation in the MYH10 gene.
Definition from the Mondo Disease Ontology (MONDO:0700281), read 2026-09-29. CC BY 4.0.
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.
- MYH10HGNC:7568
- Moderate · G2P · Autosomal dominant · 2025