solute carrier family 9 member A7
OMIM: 300368, Gene2Phenotype
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| SLC9A7 in Congenital Disorders of Glycosylation
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females | Sources
 Phenotypes
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| SLC9A7 in Mendeliome
                    
                    
                     | 2 reviews | X-LINKED: hemizygous mutation in males, biallelic mutations in females | Sources
 Phenotypes
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| SLC9A7 in Intellectual disability syndromic and non-syndromic
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females | Sources
 Phenotypes
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