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(HPO:0001743) | Abnormality of the spleen | 37 / 7739 | ||||
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(HPO:0002719) | Recurrent infections | 107 / 7739 | ||||
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(OMIM) | Congenital tuftsin deficiency | 1 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |