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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Angiomatosis +     
Fibrosis +     
aceruloplasminemia  
agenesis of the corpus callosum with peripheral neuropathy  
bacillary angiomatosis 
BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS  
breast angiomatosis +  
Cardiac Fibrosis  
Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy  
Childhood-onset Neurodegeneration with Ataxia, Tremor, Optic Atrophy, and Cognitive Decline  
Childhood-Onset Neurodegeneration with Brain Atrophy  
Childhood-Onset Neurodegeneration with Cerebellar Atrophy  
Cholangiofibrosis  
Chronic Traumatic Encephalopathy 
Cicatrix +   
congenital fibrosis of the extraocular muscles +   
demyelinating disease +   
Dermal Fibrosis  
Diffuse Corticomeningeal Angiomatosis of Divry and Van Bogaert 
eye degenerative disease +   
Familial Capillaro-Venous Leptomeningeal Angiomatosis 
Feigenbaum Bergeron Richardson Syndrome 
FINCA Syndrome  
Hapnes Boman Skeie Syndrome 
hereditary ataxia +   
Huntington's disease-like 2  
Idiopathic Basal Ganglia Calcification 1  
Idiopathic Basal Ganglia Calcification 6  
Idiopathic Basal Ganglia Calcification 7  
Klippel-Trenaunay syndrome  
LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME  
liver cirrhosis +   
motor neuron disease +   
multiple system atrophy +   
myoclonic cerebellar dyssynergia +  
Nephrogenic Fibrosing Dermopathy  
Nervous System Heredodegenerative Disorders +   
Nervous System Paraneoplastic Syndromes +   
Neurodegeneration with Ataxia and Late-Onset Optic Atrophy  
neurodegeneration with brain iron accumulation +   
NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA  
NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE  
Neuronal Intranuclear Inclusion Disease  
olivopontocerebellar atrophy +   
PEHO syndrome  
Peritoneal Fibrosis  
plexopathy 
pontocerebellar hypoplasia +   
postpoliomyelitis syndrome 
primary cerebellar degeneration +   
prion disease +   
Pseudoangiomatous Stromal Hyperplasia 
pulmonary fibrosis +   
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant 
Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression  
renal fibrosis +   
Retroperitoneal Fibrosis +   
secondary Parkinson disease +   
SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS  
Spastic Pseudosclerosis 
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
Sturge-Weber syndrome +   
Subacute Combined Degeneration  
Subretinal Fibrosis  
synucleinopathy +   
tauopathy +   
TDP-43 Proteinopathies +   
von Hippel-Lindau disease  

Synonyms
Exact Synonyms: FINCA ;   fibrosis, neurodegeneration, and cerebral angiomatosis
Primary IDs: OMIM:618278

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