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MIM:612284 - MECKEL SYNDROME, TYPE 6; MKS6
Xenbase Genes: cc2d2a
Human Disease Resource: MIM
| MONDO:0012848 - Meckel syndrome, type 6 |
| MONDO:0018921 - Meckel syndrome |
| DOID:0070120 - Meckel syndrome 6 |
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| MONDO:0012848 - Meckel syndrome, type 6 |
| MONDO:0018921 - Meckel syndrome |
| DOID:0070120 - Meckel syndrome 6 |