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GTR Home > Conditions/Phenotypes > Meckel syndrome, type 4

Meckel syndrome, type 4

Synonyms
CEP290-Related Meckel Syndrome; MECKEL-GRUBER SYNDROME, TYPE 4

Summary

Meckel syndrome is an autosomal recessive pre- or perinatal lethal disorder characterized by a combination of renal cysts and variably associated features including developmental anomalies of the central nervous system (typically occipital encephalocele), hepatic ductal dysplasia and cysts, and postaxial polydactyly (summary by Baala et al., 2007). For a more complete phenotypic description and information on genetic heterogeneity of Meckel syndrome, see MKS1 (249000). [from OMIM]

Available tests

112 tests are in the database for this condition.

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Clinical tests (112 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: 3H11Ag, BBS14, CT87, JBTS5, LCA10, MKS4, NPHP6, POC3, SLSN6, rd16, CEP290
    Summary: centrosomal protein 290

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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