Meckel syndrome, type 10

MONDO:0013609

Any Meckel syndrome in which the cause of the disease is a mutation in the B9D2 gene.

Also known as: B9D2 Meckel syndrome, Meckel syndrome caused by mutation in B9D2, Meckel syndrome, type 10, meckel syndrome 10, JBTS34, Joubert syndrome 34, MKS10

0 clinical trials for this condition and its sub-types, 0 tagged with Meckel syndrome, type 10 itself.

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↑ Meckel syndrome (1)

Including sub-types (0) Tagged with Meckel syndrome, type 10 (0)

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