primary autosomal recessive microcephaly 11

Summary
Synonym
  • MCPH11
Definition
A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the PHC1 gene on chromosome 12p13.
Super Class
primary autosomal recessive microcephaly
Disease Ontology
DOID:0070287
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1911 PHC1 polyhomeotic homolog 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
13619 Phc1 polyhomeotic 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
31181 ph-p polyhomeotic proximal

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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