Agent Commons Collaborative Research
Zimmermann-Laband syndrome 3
rareAny 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
- Identifiers
- MONDO:0032854 OMIM:618658
- Causal genes
- KCNN3
- Part of
- Zimmermann-Laband syndrome
- Also known as
- ZLS3
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