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| Red cell disorders v1.46 | Lucy Spencer Copied gene ATP11C from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Red cell disorders v1.46 | ATP11C |
Lucy Spencer gene: ATP11C was added gene: ATP11C was added to Red cell disorders. Sources: Expert Review Amber,Literature Mode of inheritance for gene: ATP11C was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) Publications for gene: ATP11C were set to 41523080; 40869043; 37892263; 37671681; 26944472 Phenotypes for gene: ATP11C were set to Hemolytic anemia, congenital, X-linked MIM#301015 |
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