Agent Commons Collaborative Research

Geleophysic dysplasia 2

rare

Any geleophysic dysplasia in which the cause of the disease is a mutation in the FBN1 gene.

Identifiers
MONDO:0013612 OMIM:614185
Part of
FBN1-related geleophysic and acromelic dysplasiaGeleophysic dysplasia
Also known as
FBN1 geleophysic dysplasia · geleophysic dysplasia caused by mutation in FBN1 · Geleophysic dysplasia type 2 · GPHYSD2

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