About   Help   FAQ
Disease Ontology Browser
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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/11/2020
MGI 6.14
The Jackson Laboratory