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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Accessory Deep Peroneal Nerve 
Acrodynia 
A condition seen primarily in childhood, most often resulting from chronic exposure to MERCURY COMPOUNDS which may result in encephalopathy and POLYNEUROPATHY. Clinical features include pain, swelling and pinkish discoloration of the fingers and toes, weakness in the extremities, extreme irritability, HYPERESTHESIA, and alterations in level of consciousness. (From Menkes, Textbook of Child Neurology, 5th ed, p603)
agenesis of the corpus callosum with peripheral neuropathy  
Amyloid Neuropathies +   
Apical Hypertrophic Cardiomyopathy and Neuropathy  
autoimmune disease of peripheral nervous system +   
autonomic nervous system disease +   
Cataract Ataxia Deafness 
Cauda equina syndrome 
complex regional pain syndrome +  
Congenital Myopathy with Neuropathy and Deafness  
Congenital Pain Insensitivity +   
diabetic neuropathy +   
Gamstorp-Wohlfart syndrome  
Hand-Arm Vibration Syndrome 
Harel-Yoon Syndrome  
Hypertrophic Neuropathy and Cataract 
Inherited Peripheral Neuropathy +   
Intellectual Developmental Disorder with Speech Delay and Axonal Peripheral Neuropathy  
leprosy +   
lumbosacral plexus lesion 
mitochondrial DNA depletion syndrome 6  
mononeuropathy +   
nerve compression syndrome +   
Neuralgia +   
neuritis +   
neuropathy +   
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Painful Neuropathy  
Peripheral Nerve Injuries  
peripheral nervous system neoplasm +   
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
polyneuropathy +   
radiculopathy +   
Sacral Plexopathy 
Small Fiber Neuropathy  
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy 
Tarlov Cysts 

Synonyms
Exact Synonyms: Acrodynic Erythema ;   Chronic Childhood Mercurialism ;   Chronic Childhood Mercurialisms ;   Feer Disease ;   Feer's Disease ;   Feers Disease ;   Pink Disease ;   Swift Disease ;   Swift's Disease ;   Swifts Disease
Primary IDs: MESH:D000170 ;   RDO:0004717
Definition Sources: MESH:D000170

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