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Ontology Browser

Term:
Congenital Cerebral Granulomas (DOID:9000851)
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Parent Terms Term With Siblings Child Terms
brain disease +     
Granuloma +     
Acute Febrile Encephalopathy 
akinetic mutism 
alveolar echinococcosis  
amblyopia +   
Athabaskan brainstem dysgenesis syndrome  
basal ganglia disease +   
baylisascariasis 
Beta-Ureidopropionase Deficiency  
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 disease +   
cerebral degeneration +   
cerebritis 
cerebrovascular disease +   
Chronic Brain Damage +   
Churg-Strauss syndrome  
Colpocephaly 
complex cortical dysplasia with other brain malformations +   
Congenital Cerebral Granulomas 
Crome Syndrome 
cystic echinococcosis  
Dermatoleukodystrophy 
diabetic encephalopathy  
disease of mental health +   
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  
Eosinophilic Granuloma  
epilepsy +   
Giant Cell Granuloma +   
granuloma annulare 
Granuloma, Foreign-Body  
Granuloma, Plasma Cell  
Headache Disorders +   
hepatic encephalopathy +   
heterophyiasis 
hypoglycemic coma 
hypothalamic disease +   
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES  
intracranial hypertension +   
intracranial hypotension 
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Kimura disease 
Kuzniecky Andermann Syndrome 
lacrimal passage granuloma 
Leukoencephalopathies +   
lymphocytic choriomeningitis  
Metabolic Brain Diseases +   
Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization  
movement disease +   
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
Necrobiotic Xanthogranuloma 
Neonatal Severe Encephalopathy with Lactic Acidosis and Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH CARDIOMYOPATHY, SPASTICITY, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH CEREBRAL ATROPHY AND VARIABLE FACIAL DYSMORPHISM  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND BRAIN ABNORMALITIES 
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
neuroschistosomiasis 
Non-Lissencephalic Cortical Dysplasia 
paragonimiasis 
phaeohyphomycosis +  
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 +   
Pseudopyogenic Granuloma 
Pyogenic Granuloma  
Rambaud Galian Syndrome 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
Respiratory Tract Granuloma +   
Sener Syndrome 
senile degeneration of brain 
Sepsis-Associated Encephalopathy  
sparganosis 
Spastic Pseudosclerosis 
Subdural Effusion 
tertiary neurosyphilis +  
thalamic disease +   
Thyrocerebral-Retinal Syndrome 
toxocariasis +   
transient global amnesia 
Wernicke encephalopathy  
Xanthogranulomatous Sialadenitis 

Synonyms
Primary IDs: MESH:C537294
Alternate IDs: OMIM:306300

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