Disease | hemophagocytic lymphohistiocytosis |
Phenotype | C0020305|hydrops fetalis |
Sentences | 1 |
PubMedID- 23073042 | Association of nonimmune hydrops fetalis with familial hemophagocytic lymphohistiocytosis in identical twin neonates with perforin his222arg (c665a>g) mutation. |
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