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Ontology Browser

Term:
Non-Lissencephalic Cortical Dysplasia (DOID:9007887)
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Parent Terms Term With Siblings Child Terms
3MC syndrome 3  
Abnormal Cortical Gyration  
Abuse Dwarfism Syndrome 
Acute Febrile Encephalopathy 
AGAT deficiency  
Akathisia, Drug-Induced 
akinetic mutism 
Al Gazali Sabrinathan Nair Syndrome 
alveolar echinococcosis  
amblyopia +   
AMED syndrome  
Angelman syndrome  
aphasia +   
Arboleda-Tham syndrome  
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
articulation disorder +   
Athabaskan brainstem dysgenesis syndrome  
Atonic-Astatic Syndrome of Foerster 
autosomal dominant mental retardation 20  
Bagatelle Cassidy syndrome 
Bainbridge-Ropers syndrome  
basal ganglia disease +   
baylisascariasis 
Beaulieu-Boycott-Innes Syndrome  
Beck-Fahrner Syndrome  
benign shuddering attacks 
Beta-Ureidopropionase Deficiency  
Bosch-Boonstra-Schaaf optic atrophy syndrome  
Brachycephaly, Trichomegaly, and Developmental Delay  
BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS  
Brain Abscess +   
brain compression  
Brain Death  
brain edema +   
Brain Hypoxia +   
Brain Injuries +   
Brain Neoplasms +   
Central Auditory Diseases +   
central nervous system origin vertigo 
Cerebellar Atrophy with Seizures and Variable Developmental Delay  
CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES  
cerebellar disease +   
cerebellar hypoplasia +   
cerebellofaciodental syndrome  
cerebral degeneration +   
cerebritis 
cerebrovascular disease +   
Chitayat Moore Del Bigio Syndrome 
Chitty Hall Webb Syndrome 
choreatic disease +   
chromosome 13q14 deletion syndrome  
chromosome 17p13.1 deletion syndrome 
chromosome 17p13.3 duplication syndrome  
chromosome 3q29 microdeletion syndrome 
chromosome Xp11.23-p11.22 duplication syndrome 
Chronic Brain Damage +   
CK syndrome  
Cleft Palate, Proliferative Retinopathy, and Developmental Delay  
Cohen syndrome  
Colpocephaly 
complex cortical dysplasia with other brain malformations +   
complex cortical dysplasia with other brain malformations 1  
Complex Cortical Dysplasia with Other Brain Malformations 10  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
complex cortical dysplasia with other brain malformations 7  
Complex Cortical Dysplasia with Other Brain Malformations 9  
Congenital Cerebral Granulomas 
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY  
congenital heart defects, dysmorphic facial features, and intellectual developmental disorder  
Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies  
congenital mirror movement disorder +   
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 
Crome Syndrome 
Curatolo Cilio Pessagno Syndrome 
cystic echinococcosis  
Der Kaloustian Mcintosh Silver Syndrome 
Dermatoleukodystrophy 
Desanto-Shinawi Syndrome  
DEVELOPMENTAL DELAY WITH DYSMORPHIC FACIES AND DENTAL ANOMALIES  
Developmental Delay with or without Dysmorphic Facies and Autism  
DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY  
DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES  
diabetic encephalopathy  
Diencephalic-Mesencephalic Junction Dysplasia Syndrome 2  
disease of mental health +   
Dyskinesias +   
Dyskinesias, Seizures, and Intellectual Developmental Disorder  
dystonia +   
echolalia 
encephalitis +   
encephalomalacia +   
Encephalopathy due to Defective Mitochondrial and Peroxisomal Fission +   
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), 8  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, 9  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM  
epilepsy +   
EPILEPSY, EARLY-ONSET, WITH OR WITHOUT DEVELOPMENTAL DELAY  
extrapyramidal and movement disease 
Faundes-Banka Syndrome  
Focal Epilepsy with Speech Disorder and with or without Mental Retardation  
Forebrain Defects  
Forsythe-Wakeling Syndrome 
Fragile Site 16p12 
Frank-Ter Haar syndrome  
GLOBAL DEVELOPMENTAL DELAY WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT  
GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES  
GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES  
Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor  
Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine  
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy 
Growth Retardation, Developmental Delay, Coarse Facies, and Early Death  
Grubben de Cock Borghgraef Syndrome 
guanidinoacetate methyltransferase deficiency  
Headache Disorders +   
hepatic encephalopathy +   
heterophyiasis 
Heyn-Sproul-Jackson Syndrome  
HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME  
hypermethioninemia due to adenosine kinase deficiency  
hypoglycemic coma 
HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT  
hypothalamic disease +   
HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME  
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
Immunodeficiency 78 with Autoimmunity and Developmental Delay  
IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA  
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES  
intracranial hypertension +   
intracranial hypotension 
Keppen-Lubinsky Syndrome  
Keratosis Follicularis Dwarfism Cerebral Atrophy 
KINSSHIP SYNDROME  
KOHLSCHUTTER-TONZ SYNDROME-LIKE  
Kuzniecky Andermann Syndrome 
Lamb-Shaffer Syndrome  
Leukoencephalopathies +   
LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME  
Li-Campeau Syndrome  
Loucks-Innes Syndrome  
Luscan-Lumish syndrome  
lymphocytic choriomeningitis  
Malformations of Cortical Development, Group I +   
Malformations of Cortical Development, Group II +   
Malformations of Cortical Development, Group III +   
Maxillofacial Dysostosis 
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome +   
Metabolic Brain Diseases +   
Microcephaly, Cataracts, Impaired Intellectual Development, and Dystonia with Abnormal Striatum  
MICROCEPHALY, DEVELOPMENTAL DELAY, AND BRITTLE HAIR SYNDROME  
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance 
microcephaly, seizures, and developmental delay  
Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia 
Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization  
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
movement disease +   
Muller Barth Menger Syndrome 
multiple system atrophy +   
mutism  
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
Neonatal Severe Encephalopathy with Lactic Acidosis and Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES, ABSENT SPEECH, AND HYPOTONIA  
NEURODEVELOPMENTAL DISORDER WITH CARDIOMYOPATHY, SPASTICITY, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH CEREBRAL ATROPHY AND VARIABLE FACIAL DYSMORPHISM  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES  
Neurodevelopmental Disorder with Impaired Speech and Hyperkinetic Movements  
neurodevelopmental disorder with involuntary movements  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES  
neuroschistosomiasis 
Nizon-Isidor Syndrome  
Non-Lissencephalic Cortical Dysplasia 
Obesity, Hyperphagia, and Developmental Delay  
Occipital Cortical Malformations  
Ogden syndrome  
Okur-Chung Neurodevelopmental Syndrome  
Oliver-McFarlane syndrome  
OPTIC ATROPHY-ATAXIA-PERIPHERAL NEUROPATHY-GLOBAL DEVELOPMENTAL DELAY SYNDROME  
Opticocochleodentate Degeneration 
Osteosclerotic Metaphyseal Dysplasia  
PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES  
pantothenate kinase-associated neurodegeneration +   
paragonimiasis 
Parkinsonism +   
Partington Anderson Syndrome 
Periventricular Nodular Heterotopia 7  
phaeohyphomycosis +  
Pierpont syndrome  
Polymicrogyria with Optic Nerve Hypoplasia  
Popov-Chang Syndrome 
prion disease +   
Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis  
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
Progressive Encephalopathy, with or without Lipodystrophy  
progressive supranuclear palsy +   
Pronation-Supination Of The Forearm, Impairment Of 
Pseudo-TORCH Syndrome +   
pseudobulbar palsy +   
Rajab Interstitial Lung Disease with Brain Calcifications +   
Rambaud Galian Syndrome 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
Refsum Disease with Increased Pipecolic Acidemia 
Rhizomelic Short Stature with Microcephaly, Micrognathia, and Developmental Delay  
Roifman-Chitayat Syndrome  
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked  
Schizencephaly  
Sener Syndrome 
senile degeneration of brain 
Sepsis-Associated Encephalopathy  
Short Stature, Developmental Delay, and Congenital Heart Defects  
SIDDIQI SYNDROME  
sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay  
Snijders Blok-Fisher Syndrome  
sparganosis 
Spastic Pseudosclerosis 
Speech Disturbance - Use of Faulty Phrasing and Unrelated Words 
speech-language disorder-1  
spondylometaphyseal dysplasia Megarbane-Dagher-Melike type  
Stiff Thumbs, with Brachydactyly Type A1 and Developmental Delay 
Stiff-Person syndrome  
Subdural Effusion 
succinic semialdehyde dehydrogenase deficiency  
Telfer Sugar Jaeger Syndrome 
tertiary neurosyphilis +  
Tetra Amelia with Ectodermal Dysplasia and Lacrimal Duct Abnormalities 
thalamic disease +   
Thyrocerebral-Retinal Syndrome 
tic disorder +   
toxocariasis +   
transient global amnesia 
Turnpenny-Fry Syndrome  
Unilateral Radioulnar Synostosis with Developmental Retardation and Hypotonia 
VERVERI-BRADY SYNDROME  
VISSERS-BODMER SYNDROME  
WEISS-KRUSZKA SYNDROME  
Wernicke encephalopathy  
Wilson disease +   

Synonyms
Primary IDs: MESH:C536243 ;   RDO:0001740

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