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MIM:206300 - ANEMIA, NONSPHEROCYTIC HEMOLYTIC, ASSOCIATED WITH ABNORMALITY OF RED CELL MEMBRANE
Xenbase Genes:
Human Disease Resource: MIM
MONDO:0008789 - cranial fossa |
DOID:2861 - congenital nonspherocytic hemolytic anemia |
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MONDO:0008789 - cranial fossa |
DOID:2861 - congenital nonspherocytic hemolytic anemia |