About   Help   FAQ
Disease Ontology Browser
pseudo-TORCH syndrome 1 (DOID:0050656)
Alliance: disease page
Synonyms: band-like calcification with simplified gyration and polymicrogyria
Alt IDs: OMIM:251290
Definition: An autosomal recessive disease that is characterized by congenital microcephaly, intracranial calcifications, severe developmental delay, severe developmental delay, simplified gyration and polymicrogyria.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
10/10/2017
MGI 6.10
The Jackson Laboratory