cerebrooculofacioskeletal syndrome 1

Summary
Definition
A cerebrooculofacioskeletal syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC6 gene on chromosome 10q11.
Super Class
cerebrooculofacioskeletal syndrome
Disease Ontology
DOID:0080911
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2074 ERCC6 ERCC excision repair 6, chromatin remodeling factor

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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