Summary
Xfe Progeroid Syndrome, is also known as xpf-ercc1 progeroid syndrome,and has symptoms including microcephaly, hearing impairment and deeply set eye. An important gene associated with Xfe Progeroid Syndrome is ERCC4 (ERCC Excision Repair 4, Endonuclease Catalytic Subunit). Affiliated tissues include skin and eye
All SNPs
Genes | SNP | Risk Alleles |
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