Meckel syndrome, type 5

MONDO:0012695

Any Meckel syndrome in which the cause of the disease is a mutation in the RPGRIP1L gene.

Also known as: MKS5, Meckel syndrome caused by mutation in RPGRIP1L, Meckel syndrome, type 5, RPGRIP1L Meckel syndrome, Meckel syndrome 5

0 clinical trials for this condition and its sub-types, 0 tagged with Meckel syndrome, type 5 itself.

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