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

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Pathways Associated With Trait

Symptoms Associated With Trait