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(HPO:0001892) | Abnormal bleeding | 85 / 7739 | ||||
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(HPO:0008354) | Factor X activation deficiency | 1 / 7739 | ||||
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(OMIM) | Platelet receptor deficiency | 1 / 7739 | ||||
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(OMIM) | Prothrombin activation deficiency | 1 / 7739 | ||||
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(OMIM) | Defect in stimulated platelet capacity to expose surface phosphatidylserine | 1 / 7739 | ||||
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(OMIM) | Impaired factor VIIIa binding | 1 / 7739 | ||||
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(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 |