FBLN5

Fibulin 5
10516

 

Cutis laxa, autosomal recessive, type IA – 219100

Charcot-Marie-Tooth disease, demyelinating, type 1H – 619764

Macular degeneration, age-related, 3 – 608895

?Cutis laxa, autosomal dominant 2 – 614434

 

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