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MIM:614078 - CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE
Xenbase Genes: bpnt2
Human Disease Resource: MIM
| MONDO:0013561 - chondrodysplasia with joint dislocations, gPAPP type |
| DOID:0112224 - chondrodysplasia with joint dislocations gPAPP type |
