primary autosomal recessive microcephaly 13

Summary
Synonym
  • MCPH13
Definition
A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CENPE gene on chromosome 4q24.
Super Class
primary autosomal recessive microcephaly
Disease Ontology
DOID:0070283
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1062 CENPE centromere protein E
Displaying 1 entry
Gene ID Gene Symbol Description Source
229841 Cenpe centromere protein E

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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