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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Auditory Neuropathy and Optic Atrophy  
An autosomal recessive neurologic disorder characterized by onset of visual and hearing impairment in the first or second decades. (OMIM)
autosomal dominant auditory neuropathy 1  
Autosomal Dominant Auditory Neuropathy 2  
autosomal dominant auditory neuropathy 3  
autosomal recessive nonsyndromic deafness 9  
Berk-Tabatznik Syndrome 
Bosch-Boonstra-Schaaf optic atrophy syndrome  
Charcot-Marie-Tooth disease X-linked recessive 5  
dominant optic atrophy plus syndrome  
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness 
GAPO syndrome  
Hagemoser Weinstein Bresnick Syndrome 
Konigsmark Knox Hussels Syndrome 
Leber hereditary optic neuropathy +   
Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy 
optic atrophy 1  
optic atrophy 10  
optic atrophy 11  
optic atrophy 12  
Optic Atrophy 13  
Optic Atrophy 14  
Optic Atrophy 15  
Optic Atrophy 16  
optic atrophy 2  
optic atrophy 3  
optic atrophy 4 
optic atrophy 5  
optic atrophy 6 
optic atrophy 7  
optic atrophy 8 
optic atrophy 9  
Optic Atrophy Spastic Paraplegia Syndrome 
Optic Atrophy with Demyelinating Disease of CNS 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
Senior-Loken syndrome +   
Spastic Paraplegia, Optic Atrophy, and Dementia 
Spastic Paraplegia, Optic Atrophy, Microcephaly, and XY Sex Reversal 
Subacute Necrotizing Encephalomyelopathy of Leigh, Adult 
Wolfram syndrome +   
X-linked deafness 5  

Synonyms
Exact Synonyms: ANOA ;   FDXR-RELATED CONDITION
Primary IDs: OMIM:617717

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