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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Hearing Loss +     
ATAXIA, PROGRESSIVE SEIZURES, MENTAL DETERIORATION, AND HEARING LOSS  
Behr syndrome  
Bilateral Hearing Loss +   
BRANCHIAL ARCH ABNORMALITIES, CHOANAL ATRESIA, ATHELIA, HEARING LOSS, AND HYPOTHYROIDISM SYNDROME  
Branchial Arch Syndrome X-Linked 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
Cataracts, Hearing Impairment, Nephrotic Syndrome, and Enterocolitis +   
chromosome 6pter-p24 deletion syndrome 
CLEFT LIP AND PALATE-CRANIOFACIAL DYSMORPHISM-CONGENITAL HEART DEFECT-HEARING LOSS SYNDROME 
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus  
Conductive Hearing Loss +   
Cone-Rod Dystrophy and Hearing Loss +   
Congenital Cataracts, Hearing Loss, and Neurodegeneration  
Deafness +   
A general term for the complete loss of the ability to hear from both ears.
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Deafness-Craniofacial Syndrome 
Ehlers-Danlos syndrome kyphoscoliotic type 2  
Functional Hearing Loss 
Hearing Loss, Mixed Conductive-Sensorineural +  
High-Frequency Hearing Loss +   
Iris Dysplasia Hypertelorism Deafness 
LADD 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 Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS AND SPASTICITY  
neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities  
neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss  
Odontochondrodysplasia 2 with Hearing Loss and Diabetes  
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Osteootohepatoenteric Syndrome  
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
Reardon Wilson Cavanagh Syndrome 
sensorineural hearing loss +   
short stature, hearing loss, retinitis pigmentosa, and distinctive facies  
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness 
syndromic X-linked intellectual disability Abidi type 
Unilateral Hearing Loss +   
uveal coloboma-cleft lip and palate-intellectual disability  
 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
 Absence of Tibia with Congenital Deafness 
 Albinism Deafness Syndrome 
 Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
 autosomal dominant congenital deafness with onychodystrophy  
 autosomal dominant nonsyndromic deafness 65  
 Ayazi Syndrome 
 Branchiogenic-Deafness Syndrome 
 Burn-McKeown syndrome  
 Cardioauditory Syndrome of Sanchez Cascos 
 COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
 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  
 Coxoauricular Syndrome 
 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, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY  
 Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
 Deafness, Congenital Onychodystrophy, Recessive Form 
 DEAFNESS, CONGENITAL, AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY  
 Deafness, with Smith-Magenis Syndrome  
 Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
 Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
 Fine-Lubinsky Syndrome  
 Fountain Syndrome 
 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 
 Hypokalemic Tubulopathy and Deafness  
 ITM2B-related cerebral amyloid angiopathy 2  
 Johnson Neuroectodermal Syndrome 
 Jones Syndrome 
 Keipert syndrome  
 Keratitis-Ichthyosis-Deafness Syndrome +   
 Konigsmark Knox Hussels Syndrome 
 LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS  
 Lynch Lee Murday syndrome 
 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
 Meyenburg-Altherr-Uehlinger Syndrome 
 Microcephaly Deafness Syndrome 
 Muckle-Wells syndrome  
 multiple synostoses syndrome 1  
 Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
 Myoclonus, Cerebellar Ataxia, and Deafness 
 Nathalie Syndrome 
 Nephrosis with Deafness and Urinary Tract and Digital Malformations 
 Noninsulin-Dependent Diabetes Mellitus with Deafness  
 nonsyndromic deafness +   
 Opticocochleodentate Degeneration 
 Perrault syndrome +   
 Ramos Arroyo Clark Syndrome 
 Ribbonlike Corneal Degeneration with Deafness 
 Richards-Rundle Syndrome 
 Schimke X-Linked Mental Retardation Syndrome 
 Schlegelberger Grote Syndrome 
 Secretory Diarrhea, Myopathy, and Deafness 
 Siddiqi syndrome  
 Sinoatrial Node Dysfunction and Deafness  
 spastic paraplegia with deafness 
 temtamy preaxial brachydactyly syndrome  
 Tietz syndrome  
 Wright Dyck Syndrome 
 X-linked Alport syndrome  
 X-linked mental retardation Gustavson type  
 X-linked mental retardation-hypotonic facies syndrome-1  
 X-linked retinitis pigmentosa and sinorespiratory infections  
 Yemenite Deaf-Blind Hypopigmentation Syndrome 

Synonyms
Exact Synonyms: Acquired Deafness ;   Bilateral Deafness ;   Complete Hearing Loss ;   Deaf Mutism ;   Extreme Hearing Loss ;   Prelingual Deafness
Narrow Synonyms: DEAFNESS WITH ANATOMICAL INNER EAR ANOMALIES
Xrefs: EFO:0001063 ;   MESH:D003638 ;   NCI:C27644
Definition Sources: MESH:D003638

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