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Ontology Browser
Term:
eyelid degenerative disease (DOID:10120)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
eyelid disease +     
neurodegenerative disease +     
aceruloplasminemia  
agenesis of the corpus callosum with peripheral neuropathy  
Barber-Say syndrome  
blepharitis +   
blepharochalasis 
blepharophimosis +   
blepharospasm +   
BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS  
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  
Chronic Traumatic Encephalopathy 
cryptophthalmia +   
Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome  
demyelinating disease +   
Eccrine Syringofibroadenomatosis with Eyelid Abnormalities 
ectropion +   
entropion +  
Epiblepharon of Upper Lid 
eversion of lacrimal punctum 
eye degenerative disease +   
eyelid benign neoplasm +   
eyelid carcinoma 
eyelid degenerative disease +  
familial isolated trichomegaly  
Feigenbaum Bergeron Richardson Syndrome 
filarial elephantiasis 
FINCA Syndrome  
hereditary ataxia +   
hordeolum +  
Huntington's disease-like 2  
hyperpigmentation of eyelid 
Idiopathic Basal Ganglia Calcification 1  
Idiopathic Basal Ganglia Calcification 6  
Idiopathic Basal Ganglia Calcification 7  
lacrimal passage granuloma 
lagophthalmos +  
LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME  
motor neuron disease +   
multiple system atrophy +   
myoclonic cerebellar dyssynergia +  
Nervous System Heredodegenerative Disorders +   
Nervous System Paraneoplastic Syndromes +   
neurodegeneration with brain iron accumulation +   
NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA  
NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE  
Neurodevelopmental Disorder with Epilepsy, Spasticity, and Brain Atrophy  
Neuronal Intranuclear Inclusion Disease  
olivopontocerebellar atrophy +   
PEHO syndrome  
plexopathy 
pontocerebellar hypoplasia +   
postpoliomyelitis syndrome 
primary cerebellar degeneration +   
prion disease +   
ptosis +   
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant 
Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression  
secondary Parkinson disease +   
SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS  
Spastic Pseudosclerosis 
stenosis of lacrimal passage 
stenosis of lacrimal punctum 
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
Subacute Combined Degeneration  
synucleinopathy +   
tauopathy +   
TDP-43 Proteinopathies +   
Trichiasis +   
vitreous disease +   

Synonyms
Exact Synonyms: eyelid degenerative diseases
Primary IDs: RDO:9002613
Xrefs: ICD9CM:374.50

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