Extremely rare human congenital disorder characterized by a full-thickness cleft within the cerebral hemispheres. These clefts are lined with gray matter and most commonly involve the parasylvian regions. Large portions of the cerebral hemispheres may be absent and replaced by cerebro-spinal fluid.

Name Development Level Target Family
Name Description
TCRDv4.6.10
UniProt Disease
DisGeNET
CLINVAR
ORPHANET