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Proximal symphalangism
MONDO:0008511Proximal symphalangism is a very rare, genetic bone disorder characterized by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive hearing loss in some patients.
Also known as: proximal symphalangism, proximal symphalangism (disease), symphalangism, Cushing type, Strasburger-Hawkins-Eldridge syndrome, Strasburger-Hawkins-Eldridge-Hargrave-McKusick syndrome, hereditary absence of proximal interphalangeal joints, hereditary absence of the proximal interphalangeal joints, vessel’s syndrome
2 clinical trials for this condition and its sub-types.
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Broader categories
Disease
(717)
Musculoskeletal system disorder
(214)
Hereditary disease
(188)
Human disease
(15)
Developmental defect during embryogenesis
(8)
Skeletal system disorder
(4)
Congenital limb malformation
(3)
Disease of genetic or genomic mechanism
(2)
Autosomal dominant disease
(0)
Autosomal genetic disease
(0)