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MIM:166000 - ENCHONDROMATOSIS, MULTIPLE, OLLIER TYPE
Xenbase Genes: pth1r
Human Disease Resource: MIM
| MONDO:0008145 - Ollier disease |
| MONDO:0013808 - Maffucci syndrome |
| DOID:4624 - Ollier disease |
|
| MONDO:0008145 - Ollier disease |
| MONDO:0013808 - Maffucci syndrome |
| DOID:4624 - Ollier disease |