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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Hearing Loss +     
inner ear disease +     
Behr syndrome  
Bilateral Hearing Loss +   
bilateral hyperactive labyrinth 
Branchial Arch Syndrome X-Linked 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
chromosome 6pter-p24 deletion syndrome 
cochlear disease +   
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 +   
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Deafness-Craniofacial Syndrome 
Ehlers-Danlos syndrome kyphoscoliotic type 2  
endolymphatic hydrops +   
Epilepsy, Hearing Loss, and Mental Retardation Syndrome  
Functional Hearing Loss 
Hearing Loss, Mixed Conductive-Sensorineural +  
High-Frequency Hearing Loss +   
inner ear cancer +  
Iris Dysplasia Hypertelorism Deafness 
labyrinthine dysfunction +  
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  
motion sickness +  
Odontochondrodysplasia 2 with Hearing Loss and Diabetes  
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Osteootohepatoenteric Syndrome  
otitis interna +   
otosclerosis +   
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
Reardon Wilson Cavanagh Syndrome 
sensorineural hearing loss +   
An inner ear disease that is characterized by hearing loss resulting from damage to the cochlea, auditory nerve and/or brainstem. (DO)
SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES  
sparganosis 
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness 
superior semicircular canal dehiscence 
syndromic X-linked intellectual disability Abidi type 
Unilateral Deafness with Delayed Endolymphatic Hydrops  
Unilateral Hearing Loss +   
uveal coloboma-cleft lip and palate-intellectual disability  
vestibular disease +   
 Acrootoocular Syndrome 
 aminoglycoside-induced deafness  
 Ataxia, Deafness, and Cardiomyopathy 
 Athabaskan brainstem dysgenesis syndrome  
 Auditory Neuropathy, Nonsyndromic Recessive 
 autosomal dominant cerebellar ataxia, deafness and narcolepsy  
 autosomal dominant nonsyndromic deafness +   
 autosomal recessive nonsyndromic deafness +   
 autosomal recessive spinocerebellar ataxia 19  
 autosomal-mitochondrial sensorineural deafness  
 Axenfeld-Rieger Anomaly with Cardiac Defects and Sensorineural Hearing Loss 
 Ayme-Gripp syndrome  
 BADS syndrome 
 Bart-Pumphrey syndrome  
 Bartter disease type 4A  
 Bartter disease type 4b  
 Bjornstad syndrome  
 Boudhina Yedes Khiari syndrome 
 Brachydactyly, Intraventricular Septal Defect, and Deafness 
 Brown-Vialetto-Van Laere syndrome +   
 CAPOS Syndrome  
 Cataract Ataxia Deafness 
 CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA  
 Cerebellar Ataxia and Hypergonadotropic Hypogonadism 
 Cerebellar Ataxia and Neurosensory Deafness 
 Charcot-Marie-Tooth disease type 1E  
 Charcot-Marie-Tooth disease type 2J  
 Charcot-Marie-Tooth disease X-linked recessive 4  
 Chitty Hall Baraitser Syndrome 
 Chudley-Mccullough syndrome  
 Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss 
 Cochleosaccular Degeneration of the Inner Ear and Progressive Cataracts 
 Combined Pituitary Hormone Deficiency, 3  
 Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
 Congenital Deafness with Total Albinism 
 Congenital Ectodermal Dysplasia with Hearing Loss 
 corneal dystrophy-perceptive deafness syndrome  
 cortical deafness +   
 craniofacial-deafness-hand syndrome  
 Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness  
 De Hauwere syndrome 
 Deafness Oligodontia Syndrome 
 Deafness, Progressive High-Tone Neural 
 deafness-intellectual disability, Martin-Probst type syndrome  
 dilated cardiomyopathy 1J  
 distal arthrogryposis type 6 
 Distal Renal Tubular Acidosis 2 with Progressive Nerve Deafness  
 Distal Renal Tubular Acidosis 3, Autosomal Recessive  
 dominant optic atrophy plus syndrome  
 Donnai-Barrow syndrome  
 DOORS syndrome  
 EAST syndrome  
 Ectodermal Dysplasia and Neurosensory Deafness 
 Ectodermal Dysplasia, Sensorineural Hearing Loss, and Distinctive Facial Features 
 Epidermolysis Bullosa Simplex 7, with Nephropathy and Deafness  
 Ermine Phenotype 
 Fitzsimmons Walson Mellor Syndrome 
 Flynn Aird Syndrome 
 Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness 
 Gemignani Syndrome 
 Generalized Lipodystrophy with Mental Retardation, Deafness, Short Stature, and Slender Bones 
 Gonadal Dysgenesis, XX Type, with Deafness +   
 Griscelli syndrome +   
 Hearing Loss, Cisplatin-Induced  
 Hearing Loss, Noise-Induced  
 Hearing Loss, Unilateral Sensorineural  
 Heimler syndrome 1  
 HID Syndrome  
 high myopia-sensorineural deafness syndrome  
 High-Frequency Hearing Loss +   
 histiocytosis-lymphadenopathy plus syndrome  
 Hittner Hirsch Kreh Syndrome  
 Homozygous 11p15-p14 Deletion Syndrome 
 hypoparathyroidism-deafness-renal disease syndrome  
 Insulin-Like Growth Factor I Deficiency  
 Johanson-Blizzard syndrome  
 Kilquist Syndrome  
 Marshall syndrome +   
 Mid-Tone Neural Deafness 
 MUSCULAR DYSTROPHY, CONGENITAL HEARING LOSS, AND OVARIAN INSUFFICIENCY SYNDROME  
 MYH-9 related disease +   
 Nephropathy Deafness Hyperparathyroidism 
 Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia 
 Nonsyndromic Sensorineural Hearing Loss +   
 ocular albinism with sensorineural deafness  
 Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
 Otodental Dysplasia 
 Otofacioosseous-Gonadal Syndrome 
 otospondylomegaepiphyseal dysplasia, autosomal recessive  
 palmoplantar keratoderma-deafness syndrome  
 Paragangliomas with Sensorineural Hearing Loss  
 Pendred syndrome  
 Pfeiffer Kapferer Syndrome 
 Pigmentary Retinopathy and Sensorineural Deafness  
 Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
 Presbycusis +   
 Progressive Nephropathy with Deafness 
 Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness 
 Retinitis Pigmentosa Inversa with Deafness 
 Robinson Miller Bensimon Syndrome 
 Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction 
 Schaap Taylor Baraitser Syndrome 
 Sensorineural Deafness and Male Infertility  
 Sensorineural Deafness and Migraine  
 Sensorineural Deafness with Hypertrophic Cardiomyopathy  
 Sensorineural Deafness with Mild Renal Dysfunction  
 Sensorineural Deafness with Peripheral Neuropathy and Arterial Disease 
 Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth 
 Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 
 split hand-foot malformation 1 with sensorineural hearing loss  
 Spondyloepiphyseal Dysplasia, Myopia, and Sensorineural Deafness 
 spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis  
 Sudden Hearing Loss  
 thiamine-responsive megaloblastic anemia syndrome  
 Townes-Brocks syndrome +   
 Treft Sanborn Carey Syndrome 
 Tunglang Savage Bellman Syndrome 
 Usher syndrome +   
 uveal coloboma-cleft lip and palate-intellectual disability  
 VISCERAL NEUROPATHY, FAMILIAL, 2, AUTOSOMAL RECESSIVE  
 Vohwinkel syndrome  
 Wolfram syndrome 2  
 Wolfram syndrome, mitochondrial form 
 X-linked nonsyndromic deafness +   

Synonyms
Exact Synonyms: central hearing loss ;   cochlear hearing loss ;   perceptive deafness ;   perceptive hearing loss ;   perceptive hearing loss or deafness ;   sensorineural deafness ;   sensorineural hearing loss disorder ;   sensory hearing loss
Narrow Synonyms: CONGENITAL SENSORINEURAL HEARING IMPAIRMENT ;   autosomal dominant deafness with peripheral neuropathy ;   bilateral sensorineural hearing impairment ;   progressive sensorineural hearing impairment
Primary IDs: MESH:D006319
Xrefs: ICD10CM:H90.5 ;   ICD9CM:389.1 ;   NCI:C26739 ;   NCI:C34662
Definition Sources: https://medlineplus.gov/ency/article/003291.htm "DO" "DO"

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