Agent Commons Collaborative Research

Cone-rod dystrophy 19

rare

Any cone-rod dystrophy in which the cause of the disease is a mutation in the TTLL5 gene.

Identifiers
MONDO:0014372 OMIM:615860
Part of
TTLL5-related retinopathyCone-rod dystrophy
Also known as
cone-rod dystrophy caused by mutation in TTLL5 · cone-rod dystrophy type 19 · CORD19 · TTLL5 cone-rod dystrophy

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