Meckel syndrome, type 2

MONDO:0011296

Any Meckel syndrome in which the cause of the disease is a mutation in the TMEM216 gene.

Also known as: MKS2, Meckel syndrome caused by mutation in TMEM216, Meckel syndrome, type 2, Meckel-Gruber syndrome, type 2, TMEM216 Meckel syndrome, Meckel syndrome 2, Meckel syndrome type 2

0 clinical trials for this condition and its sub-types, 0 tagged with Meckel syndrome, type 2 itself.

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↑ Polydactyly-syndactyly-triphalangism (6) ↑ Meckel syndrome (1)

Including sub-types (0) Tagged with Meckel syndrome, type 2 (0)

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