primary autosomal recessive microcephaly 31 Disease Ontology Browser

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Disease Ontology Browser

primary autosomal recessive microcephaly 31 (DOID:0051074)
Alliance: disease page
Alt IDs: OMIM:621507
Definition: A primary autosomal recessive microcephaly that is characterized by progressive small head circumference and poor overall postnatal growth and that has_material_basis_in homozygous mutation in the CDK4 gene on chromosome 12q14.

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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