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Parent Node:
expandMalformations of Cortical Development (D054220)
..Starting node
..expandMalformations of Cortical Development, Group I (D065703)

       Child Nodes:
........expandCerebellar Granule Cell Hypertrophy and Megalencephaly (C563565)
........expandFocal cortical dysplasia of Taylor (C537067)
........expandMegalencephaly (D058627) Child23
........expandMicrocephaly (D008831) Child140
........expandTuberous Sclerosis (D014402) Child4



 Sister Nodes: 
..expandBAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA (OMIM:251290)
..expandCK SYNDROME (OMIM:300831)
..expandCortical Dysplasia of Taylor without Balloon Cells (C564583)
..expandCortical Dysplasia-Focal Epilepsy Syndrome (C566482)
..expandCuratolo Cilio Pessagno syndrome (C536701)
..expandFamilial schizencephaly (C538514)
..expandGrowth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy (C564264)
..expandMalformations of Cortical Development, Group I (D065703) Child172
..expandMalformations of Cortical Development, Group II (D054081) Child35
..expandMalformations of Cortical Development, Group III (D065704) Child4
..expandMegalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome (C566381)
..expandMuller Barth Menger syndrome (C537370)
..expandNon-lissencephalic cortical dysplasia (C536243)
..expandPerisylvian syndrome (C536658)
..expandPitt-Hopkins-Like Syndrome 1 (C567657)
..expandPolymicrogyria With Optic Nerve Hypoplasia (C567715)
..expandPolymicrogyria, Asymmetric (C567658)
..expandPolymicrogyria, Bilateral Frontoparietal (C564652)
..expandPolymicrogyria, Bilateral Occipital (C567201)
..expandPOLYMICROGYRIA, SYMMETRIC OR ASYMMETRIC (OMIM:610031)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:6729
Name:Malformations of Cortical Development, Group I
Definition:Cortical malformations secondary to abnormal neuronal and glial CELL PROLIFERATION or APOPTOSIS in NEUROGENESIS. This group includes congenital MICROCEPHALIES; MICROLISSENCEPHALIES, megalencephalies, HEMIMEGALENCEPHALIES and cortical dysplasias with balloon cells.
Alternative IDs:
ParentIDs:MESH:D054220
TreeNumbers:C10.500.507.400 |C16.131.666.507.400
Synonyms:Abnormal Proliferation Cortical Malformations |Cortical Malformations, Group I |Malformations Due to Abnormal Neuronal and Glial Proliferation or Apoptosis |Malformations Secondary to Abnormal Neuronal and Glial Proliferation or Apoptosis
Slim Mappings:Congenital abnormality|Nervous system disease
Reference: MedGen: D065703
MeSH: D065703
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants