Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss (DOID:9002779)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Hearing Loss +     
Hoarseness +     
muscular disease +     
Accessory Deep Peroneal Nerve 
Acrodynia 
agenesis of the corpus callosum with peripheral neuropathy  
Amyloid Neuropathies +   
Apical Hypertrophic Cardiomyopathy and Neuropathy  
Arthrogryposis +   
Asrar Facharzt Haque Syndrome  
atrophic muscular disease +   
autoimmune disease of peripheral nervous system +   
autonomic nervous system disease +   
Axial Myopathy, Late-Onset +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Behr syndrome  
Bilateral Hearing Loss +   
Branchial Arch Syndrome X-Linked 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
Carey-Fineman-Ziter syndrome  
Cataract Ataxia Deafness 
Cauda equina syndrome 
chromosome 6pter-p24 deletion syndrome 
chronic fatigue syndrome  
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus  
compartment syndrome +   
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 +   
Contracture +   
Craniomandibular Disorders +   
Deafness +   
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Deafness-Craniofacial Syndrome 
diabetic neuropathy +   
diaphragm disease +   
Dimauro Disease  
Early-Onset Myopathy with Fatal Cardiomyopathy  
Ehlers-Danlos syndrome kyphoscoliotic type 2  
eosinophilia-myalgia syndrome  
Epilepsy, Hearing Loss, and Mental Retardation Syndrome  
Erythrocyte Amp Deaminase Deficiency  
Erythrocyte Lactate Transporter Defect  
familial periodic paralysis +   
fibromyalgia +   
Fingerprint Body Myopathy 
Functional Hearing Loss 
Gamstorp-Wohlfart syndrome  
Hand-Arm Vibration Syndrome 
Harel-Yoon Syndrome  
Hearing Loss, Mixed Conductive-Sensorineural +  
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
High-Frequency Hearing Loss  
Hypertrophia Musculorum Vera 
Hypertrophic Neuropathy and Cataract 
Inherited Peripheral Neuropathy +   
Internal Anal Sphincter Myopathy 
Iris Dysplasia Hypertelorism Deafness 
Kocher-Debre-Semelaigne Syndrome 
LADD syndrome  
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
leprosy +   
lipoid proteinosis  
lumbosacral plexus lesion 
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
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 6  
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
mononeuropathy +   
Muscle Cramp +   
Muscle Rigidity +   
Muscle Spasticity +   
muscle tissue disease +   
Muscle Weakness +   
Muscular Hypoplasia, Congenital Universal, of Krabbe 
Musculoskeletal Pain +   
Myalgia +   
myofascial pain syndrome +   
Myopathic Carnitine Deficiency 
Myopathy with Lactic Acidosis, Hereditary  
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia 
myositis +   
myostatin-related muscle hypertrophy  
myotonic disease +   
Myotoxicity 
nerve compression syndrome +   
Neuralgia +   
neuritis +   
neuropathy +   
Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine 
neutral lipid storage disease +   
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Painful Neuropathy  
Pectoralis Muscle, Absence of 
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 +   
Proximal Myopathy with Focal Depletion of Mitochondria 
radiculopathy +   
Reardon Wilson Cavanagh Syndrome 
Rhabdomyolysis +   
Sacral Plexopathy 
sensorineural hearing loss +   
SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES  
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
Small Fiber Neuropathy  
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy 
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness 
syndromic X-linked intellectual disability Abidi type 
systemic primary carnitine deficiency disease  
Tarlov Cysts 
Tel Hashomer Camptodactyly Syndrome 
tendinitis +   
Treft Sanborn Carey Syndrome 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Unilateral Deafness with Delayed Endolymphatic Hydrops  
Unilateral Hearing Loss +   
Uruguay faciocardiomusculoskeletal syndrome  
uveal coloboma-cleft lip and palate-intellectual disability  
Vacuolar Myopathy  
very long chain acyl-CoA dehydrogenase deficiency  

Synonyms
Exact Synonyms: PNMHH
Primary IDs: OMIM:614369 ;   RDO:9000679

paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.