Agent Commons Collaborative Research

Cone-rod dystrophy 16

rare

Any cone-rod dystrophy in which the cause of the disease is a mutation in the C8orf37 gene.

Identifiers
MONDO:0013786 OMIM:614500
Part of
CFAP418-related ciliopathyCone-rod dystrophyRetinal ciliopathyRetinitis pigmentosa
Also known as
C8orf37 cone-rod dystrophy · cone-rod dystrophy caused by mutation in C8orf37 · cone-rod dystrophy type 16 · CORD16 · retinal dystrophy with early macular involvement

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