Zimmermann-Laband syndrome 3

MONDO:0032854

Any Zimmermann-Laband syndrome in which the cause of the disease is a mutation in the KCNN3 gene. It is characterized by developmental delay, intellectual disability, coarse face, gingival hyperplasia, and nail hypoplasia/aplasia

Also known as: ZIMMERMANN-LABAND SYNDROME 3, ZLS3

0 clinical trials for this condition and its sub-types, 0 tagged with Zimmermann-Laband syndrome 3 itself.

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Including sub-types (0) Tagged with Zimmermann-Laband syndrome 3 (0)

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