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infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly (DOID:0111262)
Alliance: disease page
Synonyms: postnatal progressive microcephaly, seizures, and brain atrophy
Alt IDs: OMIM:613668, ORDO:402364
Definition: A brain disease characterized by cerebral and cerebellar atrophy, postnatal progressive microcephaly and intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in MED17 on 11q21.


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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last database update
01/17/2023
MGI 6.22
The Jackson Laboratory