symphalangism autosomal dominant disease proximal symphalangism https://www.malacards.org/card/proximal_symphalangism MESH:C536223 proximal symphalangism (disease) hereditary absence of the proximal interphalangeal joints vessel’s syndrome proximal symphalangism (disease) Strasburger-Hawkins-Eldridge syndrome symphalangism, Cushing type DOID:0050788 Proximal 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. HP:0100264 Orphanet:3250 UMLS:C1861385 hereditary absence of proximal interphalangeal joints MONDO:0008511 OMIMPS:185800 proximal symphalangism MEDGEN:348856 GARD:0008182 icd11.foundation:49802338 Strasburger-Hawkins-Eldridge-Hargrave-McKusick syndrome congenital limb malformation