phosphate regulating endopeptidase homolog X-linked
OMIM: 300550, Gene2Phenotype
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PHEX in Craniosynostosis
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1 review | Other |
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Phenotypes
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PHEX in Mendeliome
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1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) |
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Phenotypes
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PHEX in Calcium and Phosphate disorders
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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
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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
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1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) |
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Phenotypes
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PHEX in Genomic newborn screening: BabyScreen+
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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
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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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