Geleophysic dysplasia 2

MONDO:0013612

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

Also known as: FBN1 geleophysic dysplasia, Geleophysic dysplasia 2, Geleophysic dysplasia type 2, geleophysic dysplasia caused by mutation in FBN1, GELEOPHYSIC dysplasia 2, GPHYSD2

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Broader categories

Disease (717) Musculoskeletal system disorder (214) Hereditary disease (188) Bone disorder (51) Human disease (15) Skeletal system disorder (4) Disease of genetic or genomic mechanism (2) Skeletal dysplasia (1) Acromelic dysplasia (0) Disease by body system or component (0)

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