MeSH Browser

MeSH Heading: Malformations of Cortical Development, Group II
Tree Number(s): C10.500.507.450; C16.131.666.507.450
Unique ID: D054081
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D054081
Scope Note: Cortical malformations secondary to abnormal neuronal CELL MIGRATION in NEUROGENESIS. This group includes COBBLESTONE LISSENCEPHALY and PERIVENTRICULAR NODULAR HETEROTOPIA.
Entry Term(s): Cortical Malformations, Group II; Malformations Due to Abnormal Neuronal Migration; Malformations Secondary to Abnormal Neuronal Migration; Neuronal Migration Disorders
Public MeSH Note: 2008; was Neuronal Migration Disorders (2008-2014)
History Note: 2015(2008)
Date Established: 2008/01/01
Date of Entry: 2007/07/09
Revision Date: 2014/06/13

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Malformations of Cortical Development, Group II MeSH Descriptor Data 2024