Descriptor English: | Malformations of Cortical Development, Group II | ||||||
Descriptor Spanish: |
Malformaciones del Desarrollo Cortical del Grupo II
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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 |
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Tree number(s): |
C10.500.507.450 C16.131.666.507.450 |
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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. |
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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 |
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Public MeSH Note: | 2008; was Neuronal Migration Disorders (2008-2014) |
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History Note: | 2015(2008) |
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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 |
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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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