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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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory