FAM216A

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Description

The FAM216A (family with sequence similarity 216 member A) is a protein-coding gene located on chromosome 12.

FAM216A is also known as C12orf24, HSU79274.

Associated Diseases

• early-onset non-syndromic cataract
• isolated ectopia lentis
• hereditary hyperferritinemia with congenital cataracts
• cataract 13 with adult I phenotype
• cataract 38
• cataract
• cochleosaccular degeneration-cataract syndrome
• X-linked endothelial corneal dystrophy
• congenital cataract-ichthyosis syndrome
• Lisch epithelial corneal dystrophy