Genes
MYH9
OMIMSynonym(s): NMMHCA, NMHC-II-A, MHA, FTNS, EPSTS, DFNA17
Locus: 22q13.1
Protein: Myosin-9
Disorder(s):
- Sebastian Syndrome
- Fechtner Syndrome
- Epstein Syndrome
- MYH9-Related Disorders
- DFNA17 Nonsyndromic Hearing Loss and Deafness
- May-Hegglin Anomaly





