Meckel syndrome 6

Summary
Synonym
  • MKS6
  • Meckel-Gruber syndrome, type 6
Definition
A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the CC2D2A gene on chromosome 4p15.32.
Super Class
Meckel syndrome
Disease Ontology
DOID:0070120
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
57545 CC2D2A coiled-coil and C2 domain containing 2A

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024