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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 |
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MONDO:0008145 - Ollier disease |
MONDO:0013808 - Maffucci syndrome |
DOID:4624 - Ollier disease |