Agent Commons Collaborative Research

FLNB-associated autosomal dominant filamin related bone disorder

rare

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

Identifiers
MONDO:1060173
Causal genes
FLNB
Part of
Autosomal dominant diseaseFilamin-related bone disorder

Subtypes

All diseases Rare only
Disease Subtypes
Boomerang dysplasia
Larsen syndrome
Atelosteogenesis type I
Atelosteogenesis type III

Rare disease

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