DiseaseID 14188
皮质发育畸形，II型
disease
NCI2016_NICHD_1602D:A developmental brain abnormality characterized by abnormal migration of neurons during cortical development.|NCI2016_02D:A diverse group of congenital brain developmental disorders characterized by d
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 14188
- Core Entity Id
- 71937
- Source Entity Count
- 1
- Preferred Name
- Malformations of Cortical Development, Group Ii
- Name Cn
- 皮质发育畸形，II型
- Name Pinyin
- Pi Zhi Fa Yu Ji Xing ，ii Xing
- Name En
- Malformations of Cortical Development, Group Ii
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
- Do Class
- Hpo Class
- Abnormality of the nervous system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
- Hpo Class Name
- Abnormality of the nervous system
- Do Class Name
- Disease Definition
- NCI2016_NICHD_1602D:A developmental brain abnormality characterized by abnormal migration of neurons during cortical development.|NCI2016_02D:A diverse group of congenital brain developmental disorders characterized by defects in neuronal migration in the brain during early fetal development. The neuronal migration defects result in brain abnormalities that are usually manifested with mental retardation and epilepsy.|MSH2017_2016_08_12:Cortical malformations secondary to abnormal neuronal CELL MIGRATION in NEUROGENESIS. This group includes COBBLESTONE LISSENCEPHALY and PERIVENTRICULAR NODULAR HETEROTOPIA.|HPO2016_07_04:An abnormality resulting from an anomaly of neuronal migration, i.e., of the process by which neurons travel from their origin to their final position in the brain. [HPO:probinson]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Malformations of Cortical Development, Group Ii
Role
preferred
Name
Abnormal Neuronal Migration
Role
alias
Name
Abnormality of Neuronal Migration
Role
alias
Name
Heterotopias/Abnormal Migration
Role
alias
Name
Migrational Brain Disorder
Role
alias
Name
Neuronal Migration Disorder
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0002269
Herb
HBDIS015544
Me Sh
D054081
Umls
C1837249
Sym Map
SMDE10661
Dis Ge Net
C1837249
Umls Sty
T019
Hpo Class
HP:0000707
Me Sh Class
C10C16
Tcmbank Disease
17169
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Hpo Class Name
Abnormality of the nervous system
Hpo Disease Class
Abnormality of the nervous system
Umls Disease Type
Congenital Abnormality
Disease Definition
NCI2016_NICHD_1602D:A developmental brain abnormality characterized by abnormal migration of neurons during cortical development.|NCI2016_02D:A diverse group of congenital brain developmental disorders characterized by defects in neuronal migration in the brain during early fetal development. The neuronal migration defects result in brain abnormalities that are usually manifested with mental retardation and epilepsy.|MSH2017_2016_08_12:Cortical malformations secondary to abnormal neuronal CELL MIGRATION in NEUROGENESIS. This group includes COBBLESTONE LISSENCEPHALY and PERIVENTRICULAR NODULAR HETEROTOPIA.|HPO2016_07_04:An abnormality resulting from an anomaly of neuronal migration, i.e., of the process by which neurons travel from their origin to their final position in the brain. [HPO:probinson]
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Congenital Abnormality