family with sequence similarity 50 member A
OMIM: 300453, Gene2Phenotype
| Panel | Reviews | Mode of inheritance | Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| FAM50A in Mendeliome
                    
                    
                     | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| FAM50A in Genetic Epilepsy
                    
                    
                       | 2 reviews | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| FAM50A in Intellectual disability syndromic and non-syndromic
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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