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Descriptor English: Malformations of Cortical Development, Group II
Descriptor Spanish: Malformaciones del Desarrollo Cortical del Grupo II
Descriptor malformaciones del desarrollo cortical de grupo II
Entry term(s) trastornos de la emigración neuronal
Scope note: Malformaciones corticales debidas a defectos de la EMIGRACIÓN CELULAR durante la NEUROGÉNESIS. Este grupo comprende la LISENCEFALIA EN EMPEDRADO y LA HETEROTOPIA NODULAR PERIVENTRICULAR.
Descriptor Portuguese: Malformações do Desenvolvimento Cortical do Grupo II
Descriptor French: Malformations corticales du groupe II
Entry term(s): Cortical Malformations, Group II
Disorder, Neuronal Migration
Disorders, Neuronal Migration
Malformations Due to Abnormal Neuronal Migration
Malformations Secondary to Abnormal Neuronal Migration
Migration Disorder, Neuronal
Migration Disorders, Neuronal
Neuronal Migration Disorder
Neuronal Migration Disorders
Tree number(s): C10.500.507.450
C16.131.666.507.450
RDF Unique Identifier: https://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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 2008; was Neuronal Migration Disorders (2008-2014)
History Note: 2015(2008)
DeCS ID: 52597
Unique ID: D054081
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2008/01/01
Date of Entry: 2007/07/09
Revision Date: 2014/06/13
Malformations of Cortical Development, Group II - Preferred
Concept UI M0501350
Scope note Cortical malformations secondary to abnormal neuronal CELL MIGRATION in NEUROGENESIS. This group includes COBBLESTONE LISSENCEPHALY and PERIVENTRICULAR NODULAR HETEROTOPIA.
Preferred term Malformations of Cortical Development, Group II
Entry term(s) Cortical Malformations, Group II
Disorder, Neuronal Migration
Disorders, Neuronal Migration
Malformations Due to Abnormal Neuronal Migration
Malformations Secondary to Abnormal Neuronal Migration
Migration Disorder, Neuronal
Migration Disorders, Neuronal
Neuronal Migration Disorder
Neuronal Migration Disorders



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