primary autosomal dominant microcephaly 18 Disease Ontology Browser

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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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