Seckel syndrome 10

MONDO:0014991

Any Seckel syndrome in which the cause of the disease is a mutation in the NSMCE2 gene.

Also known as: NSMCE2 Seckel syndrome, SCKL10, Seckel syndrome 10, Seckel syndrome caused by mutation in NSMCE2, Seckel syndrome type 10

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

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