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FLNB-associated autosomal dominant filamin related bone disorder

MONDO:1060173

Any autosomal dominant filamin related bone disorder in which the cause of the disease is a variation in FLNB gene.

Also known as: FLNB-associated autosomal dominant filamin related bone disorder

0 clinical trials for this condition and its sub-types.

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Sub-types

Atelosteogenesis type I (0) Atelosteogenesis type III (0) Boomerang dysplasia (0) Larsen syndrome (0)

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) Autosomal dominant disease (0) Autosomal genetic disease (0)

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