| Disease | splenomegaly |
| Phenotype | C0002880|autoimmune haemolytic anaemia |
| Sentences | 1 |
| PubMedID- 21382177 | Casp10 is known as a causative gene for autoimmune lymphoproliferative syndrome (alps) type iia, another childhood syndrome of lymphadenopathy and splenomegaly associated with autoimmune haemolytic anaemia and thrombocytopenia. |
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