primary autosomal recessive microcephaly 21 Disease Ontology Browser

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Disease Ontology Browser

primary autosomal recessive microcephaly 21 (DOID:0051032)
Alliance: disease page
Alt IDs: OMIM:617983
Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous mutation in the NCAPD2 gene on chromosome 12p13.

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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