About   Help   FAQ
Disease Ontology Browser
primary autosomal dominant microcephaly 18 (DOID:0070295)
Alliance: disease page
Synonyms: MCPH18
Alt IDs: OMIM:617520
Definition: A primary microcephaly that has_material_basis_in heterozygous mutation in the WDFY3 gene on chromosome 4q21.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/12/2019
MGI 6.13
The Jackson Laboratory