primary autosomal recessive microcephaly 5 Disease Ontology Browser

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Disease Ontology Browser

primary autosomal recessive microcephaly 5 (DOID:0070280)
Alliance: disease page
Synonyms: MCPH5
Alt IDs: OMIM:608716
Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the ASPM gene on chromosome 1q31.

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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