Kleefstra syndrome 1

MONDO:0027407

An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of EHMT1 on chromosome 9q34.3.

Also known as: 9q-syndrome, KLEFS1, Kleefstra syndrome, chromosome 9q34.3 deletion syndrome, Kleefstra syndrome 1

0 clinical trials for this condition and its sub-types, 0 tagged with Kleefstra syndrome 1 itself.

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Sub-types of Kleefstra syndrome 1

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