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PedAM

Pediatric Disease Annotations & Medicines




Disease splenomegaly
Phenotype C0002880|autoimmune haemolytic anaemia
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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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