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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.13
The Jackson Laboratory