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Ontology Browser

Term:
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant (DOID:9001964)
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Parent Terms Term With Siblings Child Terms
Hearing Loss +     
optic atrophy +     
3-methylglutaconic aciduria type 3  
Accessory Deep Peroneal Nerve 
Acrodynia 
agenesis of the corpus callosum with peripheral neuropathy  
Al Gazali Khidr Prem Chandran Syndrome 
Al Gazali Sabrinathan Nair Syndrome 
Amyloid Neuropathies +   
Apical Hypertrophic Cardiomyopathy and Neuropathy  
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION  
autoimmune disease of peripheral nervous system +   
autonomic nervous system disease +   
Behr syndrome  
Bilateral Hearing Loss +   
Branchial Arch Syndrome X-Linked 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
CAPOS Syndrome  
Cataract Ataxia Deafness 
Cauda equina syndrome 
Childhood-onset Neurodegeneration with Ataxia, Tremor, Optic Atrophy, and Cognitive Decline  
chromosome 6pter-p24 deletion syndrome 
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus  
complex regional pain syndrome +  
Conductive Hearing Loss +   
Cone-Rod Dystrophy and Hearing Loss +   
Congenital Cataracts, Hearing Loss, and Neurodegeneration  
Congenital Myopathy with Neuropathy and Deafness  
Congenital Pain Insensitivity +   
Deafness +   
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Deafness-Craniofacial Syndrome 
deafness-dystonia-optic neuronopathy syndrome  
diabetic neuropathy +   
DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES  
Ehlers-Danlos syndrome kyphoscoliotic type 2  
Epilepsy, Hearing Loss, and Mental Retardation Syndrome  
Episodic Mitochondrial Myopathy with or without Optic Atrophy and Reversible Leukoencephalopathy  
Functional Hearing Loss 
Gamstorp-Wohlfart syndrome  
glaucomatous atrophy of optic disc 
Hand-Arm Vibration Syndrome 
Harel-Yoon Syndrome  
Hearing Loss, Mixed Conductive-Sensorineural +  
Hereditary Optic Atrophies +   
High-Frequency Hearing Loss +   
Hypertrophic Neuropathy and Cataract 
infantile cerebellar-retinal degeneration  
Inherited Peripheral Neuropathy +   
Intellectual Developmental Disorder with Speech Delay and Axonal Peripheral Neuropathy  
Iris Dysplasia Hypertelorism Deafness 
LADD syndrome  
leprosy +   
lumbosacral plexus lesion 
Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature 
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance 
Microtia, Hearing Impairment, and Cleft Palate  
midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis  
MITCHELL SYNDROME  
MITOCHONDRIAL DNA DEPLETION SYNDROME 16B  
mitochondrial DNA depletion syndrome 6  
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
mononeuropathy +   
nerve compression syndrome +   
Neuralgia +   
neuritis +   
Neurodegeneration with Ataxia and Late-Onset Optic Atrophy  
NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES  
neuropathy +   
Odontochondrodysplasia 2 with Hearing Loss and Diabetes  
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
OPTIC ATROPHY-ATAXIA-PERIPHERAL NEUROPATHY-GLOBAL DEVELOPMENTAL DELAY SYNDROME  
Osteootohepatoenteric Syndrome  
Painful Neuropathy  
partial optic atrophy 
PEHO syndrome  
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 +   
primary optic atrophy 
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
radiculopathy +   
Reardon Wilson Cavanagh Syndrome 
Sacral Plexopathy 
sensorineural hearing loss +   
SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES  
Silengo Lerone Pelizza Syndrome 
Small Fiber Neuropathy  
spastic ataxia +   
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy 
SPOAN syndrome  
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness 
syndromic X-linked intellectual disability Abidi type 
Tarlov Cysts 
Treft Sanborn Carey Syndrome 
Unilateral Deafness with Delayed Endolymphatic Hydrops  
Unilateral Hearing Loss +   
uveal coloboma-cleft lip and palate-intellectual disability  
Warburg micro syndrome +   
X-Linked Mental Retardation Gustavson Type 

Synonyms
Primary IDs: MESH:C563497 ;   RDO:0012739

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