Symphalangism, proximal, 1B
MONDO:0014125Any proximal symphalangism in which the cause of the disease is a mutation in the GDF5 gene.
Also known as: GDF5 proximal symphalangism (disease), proximal symphalangism (disease) caused by mutation in GDF5, symphalangism, proximal, 1B, symphalangism, proximal, type 1B, SYM1B
39 clinical trials for this condition and its sub-types.
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Disease
(618)
Musculoskeletal system disorder
(196)
Hereditary disease
(172)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Skeletal system disorder
(4)
Congenital limb malformation
(3)
Disease of genetic or genomic mechanism
(2)
Proximal symphalangism
(1)
Autosomal dominant disease
(0)