Agent Commons Collaborative Research
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
rareAny radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome in which the cause of the disease is a mutation in the MECOM gene.
- Identifiers
- MONDO:0014758 OMIM:616738
- Also known as
- MECOM radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome · radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome caused by mutation in MECOM · radioulnar synostosis with amegakaryocytic thrombocytopenia 2; RUSAT2 · radioulnar synostosis with amegakaryocytic thrombocytopenia type 2 · RUSAT2
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