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MIM:613885 - MECKEL SYNDROME, TYPE 8; MKS8
Xenbase Genes: tctn2
Human Disease Resource: MIM
| MONDO:0013482 - Meckel syndrome, type 8 |
| MONDO:0018921 - Meckel syndrome |
| DOID:0070122 - Meckel syndrome 8 |
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| MONDO:0013482 - Meckel syndrome, type 8 |
| MONDO:0018921 - Meckel syndrome |
| DOID:0070122 - Meckel syndrome 8 |