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Term:
Myopathy, Epilepsy, and Progressive Cerebral Atrophy (DOID:9003980)
Annotations: Rat: (1) Mouse: (1) Human: (2) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
brain disease +     
epilepsy +     
myopathy +     
Acute Febrile Encephalopathy 
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
akinetic mutism 
Alcohol Myopathy  
Alopecia, Epilepsy, Pyorrhea, Mental Subnormality 
Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan 
alveolar echinococcosis  
amblyopia +   
Arthrogryposis Epileptic Seizures Migrational Brain Disorder 
Athabaskan brainstem dysgenesis syndrome  
autoimmune epilepsy 
autosomal dominant mental retardation 20  
Autosomal Dominant Mental Retardation 60  
autosomal recessive spinocerebellar ataxia 12  
Baraitser-Winter syndrome +   
basal ganglia disease +   
Battaglia Neri Syndrome 
baylisascariasis 
Beta-Amino Acids, Renal Transport of 
Beta-Ureidopropionase Deficiency  
Borjeson-Forssman-Lehmann syndrome  
Boudhina Yedes Khiari syndrome 
BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS  
Brain Abscess +   
brain compression  
Brain Death  
brain edema +   
Brain Hypoxia +   
Brain Injuries +   
Brain Neoplasms +   
branched-chain keto acid dehydrogenase kinase deficiency  
Central Auditory Diseases +   
central nervous system origin vertigo 
centronuclear myopathy +   
CEREBELLAR ATAXIA, BRAIN ABNORMALITIES, AND CARDIAC CONDUCTION DEFECTS  
Cerebellar Atrophy with Seizures and Variable Developmental Delay  
cerebellar disease +   
cerebral degeneration +   
cerebritis 
cerebrovascular disease +   
Christianson syndrome  
Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB 
Chronic Brain Damage +   
Coffin Syndrome 1 
Colpocephaly 
complex cortical dysplasia with other brain malformations +   
Congenital Cerebral Granulomas 
Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies  
congenital myopathy +   
congenital structural myopathy +   
Crome Syndrome 
cystic echinococcosis  
Dermatoleukodystrophy 
Developmental Delay, Epilepsy, and Neonatal Diabetes  
diabetic encephalopathy  
disease of mental health +   
Drug Resistant Epilepsy +   
early-onset vitamin B6-dependent epilepsy  
electroclinical syndrome +   
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 Telangiectasia 
EPILEPSY, EARLY-ONSET, WITH OR WITHOUT DEVELOPMENTAL DELAY  
Epilepsy, Hearing Loss, and Mental Retardation Syndrome  
Epilepsy, Occipital Calcifications 
Epilepsy, Post-Traumatic 
extratemporal epilepsy 
Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome  
Febrile Seizures +   
Focal Cortical Dysplasia of Taylor +   
focal epilepsy +   
Generalized Epilepsy +   
Glycosylphosphatidylinositol Deficiency +   
Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy and Myopathy  
Gurrieri Sammito Bellussi Syndrome 
Halperin-Birk Syndrome  
Headache Disorders +   
hepatic encephalopathy +   
heterophyiasis 
Hot Water Epilepsy +  
hypoglycemic coma 
hypothalamic disease +   
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES  
Intellectual Developmental Disorder with Behavioral Abnormalities and Craniofacial Dysmorphism with or without Seizures  
Intellectual Developmental Disorder with Macrocephaly, Seizures, and Speech Delay  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH POOR GROWTH AND WITH OR WITHOUT SEIZURES OR ATAXIA  
Intellectual Developmental Disorder with Seizures and Language Delay  
intracranial hypertension +   
intracranial hypotension 
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Kifafa Seizure Disorder 
King Denborough syndrome  
KINSSHIP SYNDROME  
Kohlschutter-Tonz syndrome  
Kuzniecky Andermann Syndrome 
Leukoencephalopathies +   
lymphocytic choriomeningitis  
MEHMO syndrome  
Mental Retardation, Microcephaly, Epilepsy, and Coarse Face 
Metabolic Brain Diseases +   
Microcephaly, Epilepsy, and Diabetes Syndrome +   
Microcephaly, Growth Deficiency, Seizures, and Brain Malformations  
Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization  
mitochondrial myopathy +   
movement disease +   
Multiple Epiphyseal Dysplasia with Myopathy 
muscular atrophy +   
muscular dystrophy +   
Myoclonic Epilepsies +   
myofascial pain syndrome +   
myofibrillar myopathy +   
myoglobinuria +   
Myopathy due to Malate-Aspartate Shuttle Defect 
MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  
myopathy of extraocular muscle +   
myopathy with extrapyramidal signs  
Myopathy with Giant Abnormal Mitochondria 
Myopathy, Cataract, Hypogonadism Syndrome 
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
myositis +   
Myostitis 
Neonatal Severe Encephalopathy with Lactic Acidosis and Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY  
NEURODEVELOPMENTAL DISORDER WITH CARDIOMYOPATHY, SPASTICITY, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH CEREBRAL ATROPHY AND VARIABLE FACIAL DYSMORPHISM  
Neurodevelopmental Disorder with Dysmorphic Facies and Variable Seizures  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM  
Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination  
Neurodevelopmental Disorder with Epilepsy, Spasticity, and Brain Atrophy  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES  
Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, EPILEPSY, AND GAIT ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND BRAIN ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY  
Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech, and Seizures  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND GINGIVAL OVERGROWTH  
Neurodevelopmental Disorder with Seizures and Nonepileptic Hyperkinetic Movements  
Neurodevelopmental Disorder with Seizures and Speech and Walking Impairment  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES  
neurogenic scapuloperoneal syndrome Kaeser type  
neuroschistosomiasis 
Neutral Lipid Storage Disease with Myopathy  
Non-Lissencephalic Cortical Dysplasia 
Oculopharyngeal Myopathy with Leukoencephalopathy 1  
ONYCHODYSTROPHY, OSTEODYSTROPHY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES SYNDROME  
PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES  
paragonimiasis 
phaeohyphomycosis +  
Photogenic Epilepsy with Spastic Diplegia and Mental Retardation 
Pitt-Hopkins syndrome +   
POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME  
Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy  
polymyalgia rheumatica  
prion disease +   
Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis  
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
Progressive Encephalopathy, with or without Lipodystrophy  
Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy  
Pseudo-TORCH Syndrome +   
pseudobulbar palsy +   
Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism  
pyridoxamine 5'-phosphate oxidase deficiency  
pyridoxine-dependent epilepsy  
Rambaud Galian Syndrome 
Ramon Syndrome 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
Reducing Body Myopathies +   
Retinal Degeneration and Epilepsy 
rhabdomyolysis-myalgia syndrome 
Rud Syndrome 
salt and pepper syndrome  
Sandhaus Ben-Ami Syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS  
SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  
Sener Syndrome 
senile degeneration of brain 
Sepsis-Associated Encephalopathy  
sparganosis 
Spastic Pseudosclerosis 
Spinocerebellar Ataxia with Epilepsy  
status epilepticus +   
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
Subdural Effusion 
syndromic X-linked intellectual disability Hedera type  
tertiary neurosyphilis +  
thalamic disease +   
Thyrocerebral-Retinal Syndrome 
toxocariasis +   
transient global amnesia 
Tubular Aggregate Myopathies +   
visual epilepsy +   
Webb-Dattani Syndrome  
Wernicke encephalopathy  
Wittwer Syndrome  
X-linked epilepsy with variable learning disabilities and behavior disorders  
X-linked myopathy with excessive autophagy  

Synonyms
Exact Synonyms: MEPCA
Primary IDs: OMIM:619036

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