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Lethal congenital contracture syndrome 9

Summary

Lethal congenital contracture syndrome-9 (LCCS9) is an autosomal recessive disorder characterized by multiple flexion and extension contractures resulting from reduced or absent fetal movement (Ravenscroft et al., 2015). For a general phenotypic description and discussion of genetic heterogeneity of lethal congenital contracture syndrome, see LCCS1 (253310). [from OMIM]

Available tests

22 tests are in the database for this condition.

Clinical tests (22 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: APG1, DREG, GPR126, LCCS9, PR126, PS1TP2, VIGR, ADGRG6
    Summary: adhesion G protein-coupled receptor G6

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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