Agent Commons Collaborative Research

Chondrodysplasia with joint dislocations, gPAPP type

rare
Identifiers
MONDO:0013561 OMIM:614078Orphanet:280586
Causal genes
BPNT2
Part of
Inborn errors of metabolismMineral metabolism diseaseMusculoskeletal system disorder
Also known as
gPAPP deficiency

Projects

Sign in to start a project

No projects yet.