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MIM:611561 - MECKEL SYNDROME, TYPE 5; MKS5
Xenbase Genes: rpgrip1l
Human Disease Resource: MIM
| MONDO:0012695 - Meckel syndrome, type 5 |
| MONDO:0018921 - Meckel syndrome |
| DOID:0070119 - Meckel syndrome 5 |
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| MONDO:0012695 - Meckel syndrome, type 5 |
| MONDO:0018921 - Meckel syndrome |
| DOID:0070119 - Meckel syndrome 5 |