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, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory