phosphate regulating endopeptidase homolog X-linked
OMIM: 300550, Gene2Phenotype
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| PHEX in Craniosynostosis
                    
                    
                       | 1 review | Other | Sources
 Phenotypes
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| PHEX 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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| PHEX in Calcium and Phosphate disorders
                    
                    
                       | 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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| PHEX in Skeletal dysplasia
                    
                      Level 3: Skeletal dysplasias
                    
                    
                       | 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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| PHEX in Fetal anomalies
                    
                    
                     | 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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| PHEX in Genomic newborn screening: BabyScreen+
                    
                    
                       | 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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| PHEX in Renal Tubulopathies and related disorders
                    
                    
                       | 3 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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