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Term:
complex cortical dysplasia with other brain malformations (DOID:0090131)
Annotations: Rat: (420) Mouse: (418) Human: (450) Chinchilla: (398) Bonobo: (407) Dog: (412) Squirrel: (405)
Parent Terms Term With Siblings Child Terms
Acute Febrile Encephalopathy 
Agenesis of Corpus Callosum +   
Aicardi-Goutieres syndrome +   
akinetic mutism 
alveolar echinococcosis 
amblyopia +   
Athabaskan brainstem dysgenesis syndrome  
basal ganglia disease +   
baylisascariasis 
Beta-Ureidopropionase Deficiency  
Brain Abscess +   
brain compression  
Brain Death  
brain edema +   
Brain Hypoxia +   
Brain Injuries +   
Brain Neoplasms +   
Central Auditory Diseases +   
Central Nervous System Cysts +   
central nervous system origin vertigo 
Central Nervous System Vascular Malformations +   
cerebellar disease +   
Cerebellar Hypoplasia +   
cerebral degeneration +   
cerebritis 
cerebrovascular disease +   
chromosome 17p13.3 duplication syndrome 
chromosome 1p32-p31 deletion syndrome  
Chronic Brain Damage +   
Colpocephaly  
complex cortical dysplasia with other brain malformations +   
Abnormalities in the development of the CEREBRAL CORTEX. These include malformations arising from abnormal neuronal and glial CELL PROLIFERATION or APOPTOSIS (Group I); abnormal neuronal migration (Group II); and abnormal establishment of cortical organization (Group III). Many INBORN METABOLIC BRAIN DISORDERS affecting CNS formation are often associated with cortical malformations. They are common causes of EPILEPSY and developmental delay.
Crome Syndrome 
cystic echinococcosis 
Dandy-Walker syndrome +   
dementia +   
Dermatoleukodystrophy 
diabetic encephalopathy  
disease of mental health +   
Drachtman Weinblatt Sitarz Syndrome 
encephalitis +   
encephalomalacia +   
ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), 8  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3  
ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM  
epilepsy +   
Granulomas, Congenital Cerebral 
Headache Disorders +   
HEART AND BRAIN MALFORMATION SYNDROME  
hepatic encephalopathy +   
hereditary sensory neuropathy +   
heterophyiasis 
hydrocephalus +   
hypoglycemic coma 
hypothalamic disease +   
intracranial hypertension +   
intracranial hypotension 
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Kuzniecky Andermann Syndrome 
Leukoencephalopathies +   
lymphocytic choriomeningitis  
Median-Ulnar Nerve Communications 
Metabolic Brain Diseases +   
Microcephaly, Growth Deficiency, Seizures, and Brain Malformations  
Microphthalmia, Syndromic 3  
Microphthalmia, Syndromic 6  
Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization  
movement disease +   
neural tube defect +   
Neurodevelopmental Disorder and Language Delay with or Without Structural Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION  
neurodevelopmental disorder with midbrain and hindbrain malformations  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART  
neuroschistosomiasis 
Non-Lissencephalic Cortical Dysplasia 
olfactory nerve disease +   
paragonimiasis 
phaeohyphomycosis +  
Postnatal Progressive Microcephaly with Seizures and Brain Atrophy  
prion disease +   
Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis  
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
Progressive Encephalopathy, with or without Lipodystrophy  
Pseudo-TORCH Syndrome +   
pseudobulbar palsy +  
Rajab Syndrome  
Rambaud Galian Syndrome 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
Schisis Association 
Sener Syndrome 
senile degeneration of brain 
Sepsis-Associated Encephalopathy  
septooptic dysplasia +   
sparganosis 
Spastic Pseudosclerosis 
Subdural Effusion 
tertiary neurosyphilis +  
thalamic disease +   
Thyrocerebral-Retinal Syndrome 
toxocariasis +   
transient global amnesia 
Wernicke encephalopathy  

Synonyms
Exact Synonyms: CDCBM ;   Cerebral Cortical Dysplasia ;   Cerebral Cortical Dysplasias ;   Cortical Development Malformation ;   Cortical Development Malformations ;   Cortical Dysplasia ;   Cortical Dysplasias ;   Malformations of Cerebral Cortex Development ;   Malformations of Cortical Development
Narrow Synonyms: FCD ;   Focal cortical dysplasia
Primary IDs: MESH:D054220 ;   RDO:0001743
Xrefs: OMIM:PS614039
Definition Sources: MESH:D054220

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.