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Term:
Congenital Myopathy with Neuropathy and Deafness (DOID:9007907)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Deafness +     
muscular disease +     
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
Absence of Tibia with Congenital Deafness 
Accessory Deep Peroneal Nerve 
Acrodynia 
agenesis of the corpus callosum with peripheral neuropathy  
Albinism Deafness Syndrome 
Amyloid Neuropathies +   
Apical Hypertrophic Cardiomyopathy and Neuropathy  
Arthrogryposis +   
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
atrophic muscular disease +   
autoimmune disease of peripheral nervous system +   
autonomic nervous system disease +   
autosomal dominant congenital deafness with onychodystrophy  
autosomal dominant nonsyndromic deafness 65  
Axial Myopathy, Late-Onset +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Ayazi Syndrome 
Branchiogenic-Deafness Syndrome 
Burn-McKeown syndrome  
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
Cardioauditory Syndrome of Sanchez Cascos 
Carey-Fineman-Ziter syndrome  
Cataract Ataxia Deafness 
Cauda equina syndrome 
chronic fatigue syndrome  
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
compartment syndrome +   
complex regional pain syndrome +  
Congenital Deafness and Familial Myoclonic Epilepsy 
Congenital Deafness, with Vitiligo and Achalasia 
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation 
Congenital Myopathy with Neuropathy and Deafness  
Congenital Pain Insensitivity +   
Contracture +   
Coxoauricular Syndrome 
Craniomandibular Disorders +   
Davenport Donlan Syndrome 
Deaf-Blind Disorders +   
Deafness Hyperuricemia Neurologic Ataxia 
Deafness with Anhidrotic Ectodermal Dysplasia 
Deafness, Autosomal Dominant, due to Mutation In Myo1a 
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
Deafness, Congenital Onychodystrophy, Recessive Form 
Deafness, with Smith-Magenis Syndrome  
diabetic neuropathy +   
diaphragm disease +   
Dimauro Disease  
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
Early-Onset Myopathy with Fatal Cardiomyopathy  
Ehlers-Danlos syndrome kyphoscoliotic type 2  
eosinophilia-myalgia syndrome  
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
Erythrocyte Amp Deaminase Deficiency  
Erythrocyte Lactate Transporter Defect  
familial periodic paralysis +   
fibromyalgia +   
Fine-Lubinsky Syndrome 
Fingerprint Body Myopathy 
Fountain Syndrome 
Gamstorp-Wohlfart syndrome  
Hand-Arm Vibration Syndrome 
Harel-Yoon Syndrome  
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
hereditary spastic paraplegia 24 
Herrmann Syndrome 
high myopia-sensorineural deafness syndrome  
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hyperlipoproteinemia Type II, and Deafness 
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
Hypertrophia Musculorum Vera 
Hypertrophic Neuropathy and Cataract 
Inherited Peripheral Neuropathy +   
Intellectual Developmental Disorder with Speech Delay and Axonal Peripheral Neuropathy 
Internal Anal Sphincter Myopathy 
ITM2B-related cerebral amyloid angiopathy 2  
Johnson Neuroectodermal Syndrome 
Jones Syndrome 
Keipert syndrome  
Keratitis-Ichthyosis-Deafness Syndrome +   
Kocher-Debre-Semelaigne Syndrome 
Konigsmark Knox Hussels Syndrome 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
leprosy +   
lumbosacral plexus lesion 
Lynch Lee Murday syndrome 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1  
Meyenburg-Altherr-Uehlinger Syndrome 
Microcephaly Deafness Syndrome 
mitochondrial DNA depletion syndrome 6  
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
mononeuropathy +   
Muckle-Wells syndrome  
Multiple Synostoses Syndrome 1  
Muscle Cramp +   
Muscle Rigidity +   
Muscle Spasticity +   
muscle tissue disease +   
Muscle Weakness +   
Muscular Hypoplasia, Congenital Universal, of Krabbe 
Musculoskeletal Pain +   
Myalgia +   
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonus, Cerebellar Ataxia, and Deafness 
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 
Nathalie Syndrome 
Nephrosis Deafness Urinary Tract Digital Malformation 
nerve compression syndrome +   
Neuralgia +   
neuritis +   
neuropathy +   
Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine 
neutral lipid storage disease +   
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nonsyndromic deafness +   
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Opticocochleodentate Degeneration 
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  
Perrault syndrome +   
polyneuropathy +   
Proximal Myopathy with Focal Depletion of Mitochondria 
radiculopathy +   
Ramos Arroyo Clark Syndrome 
Rhabdomyolysis +   
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Sacral Plexopathy 
Schimke X-Linked Mental Retardation Syndrome 
Schlegelberger Grote Syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
SIDDIQI SYNDROME  
Singleton Merten Syndrome +   
Sinoatrial Node Dysfunction and Deafness  
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
Small Fiber Neuropathy  
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy 
systemic primary carnitine deficiency disease  
Tarlov Cysts 
Tel Hashomer Camptodactyly Syndrome 
temtamy preaxial brachydactyly syndrome  
tendinitis +   
Tietz syndrome  
Treft Sanborn Carey Syndrome 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Uruguay faciocardiomusculoskeletal syndrome  
Vacuolar Myopathy  
very long chain acyl-CoA dehydrogenase deficiency  
Wells Jankovic Syndrome 
Wright Dyck Syndrome 
X-linked Alport syndrome  
X-Linked Mental Retardation Gustavson Type 
X-linked retinitis pigmentosa and sinorespiratory infections  
Yemenite Deaf-Blind Hypopigmentation Syndrome 

Synonyms
Exact Synonyms: CMND ;   congenital myopathy, neuropathy, and deafness
Primary IDs: OMIM:617519
Alternate IDs: RDO:9001749

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