CR1L

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Description

The CR1L (complement C3b/C4b receptor 1 like) is a protein-coding gene located on chromosome 1.

CR1L is also known as -.

Associated Diseases

• Alzheimer disease
• familial juvenile hyperuricemic nephropathy type 1
• X-linked retinal dysplasia
• severe early-childhood-onset retinal dystrophy
• age related macular degeneration 4
• age related macular degeneration 11
• age related macular degeneration 7
• xanthinuria type II
• hypoxanthine guanine phosphoribosyltransferase partial deficiency