primary autosomal recessive microcephaly 3

Summary
Synonym
  • MCPH3
Definition
A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CDK5RAP2 gene on chromosome 9q33.
Super Class
primary autosomal recessive microcephaly
Disease Ontology
DOID:0070286
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
55755 CDK5RAP2 CDK5 regulatory subunit associated protein 2

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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