primary autosomal recessive microcephaly 8

Summary
Synonym
  • MCPH8
Definition
A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CEP135 gene on chromosome 4q.
Super Class
primary autosomal recessive microcephaly
External Links
Disease Ontology
DOID:0070282
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9662 CEP135 centrosomal protein 135

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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: August 19, 2024