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radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome

Disease Summary
Associated Targets (2)
Tbio

2


Mondo Description Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome is characterised by the association of proximal fusion of the radius and ulna with congenital amegakaryocytic thrombocytopaenia. Less than 10 cases have been reported in the literature so far. The syndrome is transmitted as an autosomal dominant trait and is caused by mutations in the HOXA11 gene (7p15).
Mondo Term and Equivalent IDs
MONDO:0011555:  radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
MESH:C565328: 
OMIMPS:605432: 
Orphanet:71289: 
SCTID:721882001: