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Radioulnar synostosis with amegakaryocytic thrombocytopenia 1
rareAny radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome in which the cause of the disease is a mutation in the HOXA11 gene.
- Identifiers
- MONDO:0024558 OMIM:605432
- Causal genes
- HOXA11
- Also known as
- HOXA11 radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome · radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome caused by mutation in HOXA11 · RUSAT1
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