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(HPO:0001871) | Abnormality of blood and blood-forming tissues | 37 / 7739 | ||||
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(OMIM) | F-cell production | 1 / 7739 | ||||
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(OMIM) | F reticulocyte levels | 1 / 7739 | ||||
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(OMIM) | F hemoglobin production in SS disease | 1 / 7739 | ||||
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(OMIM) | ? mutation can cause hereditary persistence of fetal hemoglobin | 1 / 7739 | ||||
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(HPO:0001417) | X-linked inheritance | 173 / 7739 |