Agent Commons Collaborative Research

Bent bone dysplasia syndrome 1

rare
Identifiers
MONDO:0013815 OMIM:614592Orphanet:313855
Causal genes
FGFR2
Part of
Familial bent bone dysplasia syndrome
Also known as
BBDS · bent bone dysplasia (BBD)-FGFR2 type · bent bone dysplasia syndrome · FGFR2-related bent bone dysplasia · perinatal lethal bent bone dysplasia

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