Meckel syndrome, type 3

MONDO:0011821

Any Meckel syndrome in which the cause of the disease is a mutation in the TMEM67 gene.

Also known as: MKS3, Meckel syndrome caused by mutation in TMEM67, Meckel syndrome, type 3, Meckel-Gruber syndrome, type 3, TMEM67 Meckel syndrome, Meckel syndrome 3, Meckel syndrome type 3

37 clinical trials for this condition and its sub-types.

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