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| OMIM Disease Term | Gene |
| Deafness | DFNA5 |
| MYH14 | |
| ACTG1 | |
| MYH9 | |
| RDX | |
| Anemia | TPI1 |
| HK1 | |
| GSS | |
| GPI | |
| Myopathy | TPM2 |
| TPM3 | |
| FLNC | |
| Leukemia | LPP |
| NUMA1 | |
| PML |
Genes identified in the human MYH9 proteomics that are also listed in OMIM as genes that when mutated can cause human diseases. There are many more genes that overlap with entries in OMIM. Only relevant diseases for the discussion are shown.
