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Zimmermann-laband syndrome 3

Summary

Zimmermann-Laband syndrome-3 (ZLS3) is characterized by developmental delay, intellectual disability, coarse face, gingival hyperplasia, and nail hypoplasia/aplasia (Bauer et al., 2019). For a general phenotypic description and a discussion of genetic heterogeneity of Zimmermann-Laband syndrome, see ZLS1 (135500). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: KCa2.3, SK3, SKCA3, ZLS3, hSK3, KCNN3
    Summary: potassium calcium-activated channel subfamily N member 3

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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