hearing loss, sensorineural

Preferred Label : hearing loss, sensorineural;

MeSH definition : Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM.;

MeSH synonym : sensorineural hearing loss; Deafness Neurosensory; Sensoryneural Deafness; Deafnesses, Sensoryneural; Sensoryneural Deafnesses; Deafness, Neurosensory; Neurosensory Deafness; Deafnesses, Neurosensory; Neurosensory Deafnesses; Deafness, Sensoryneural;

MeSH hyponym : hearing loss, cochlear; Cochlear Hearing Loss;

MeSH annotation : HEARING LOSS, MIXED CONDUCTIVE-SENSORINEURAL is also available;

Wikipedia link : https://en.wikipedia.org/wiki/Sensorineural hearing loss;

Details

Origin ID

D006319;

UMLS CUI

C0018784;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- COCHLEAR NERVE DEAFNESS [WHO-ART Included Term]
- Sensorineural hearing impairment [HPO term]
- Sensorineural hearing loss [ICD-9 code]
- Sensory hearing loss [PASCAL descriptor]
Currated CISMeF NLP mapping
- Acquired sensorineural hearing loss [ICD-11 Subcategory]
- Deafness neurosensory [MedDRA Preferred Term]
- Neuro sensory deafness [MedDRA LLT]
- Perception hearing loss [PASCAL descriptor]
- Perceptive deafness [MedDRA LLT]
- Sensorineural Hearing Loss [NCIt concept]
- Sensorineural deafness [HPO term]
- Sensorineural deafness [MedDRA LLT]
- Sensorineural hearing loss [MedDRA LLT]
- Sensorineural hearing loss (disorder) [SNOMED CT concept]
- Sensorineural hearing loss, unspecified [ICD-10 Sub-category (who)]
- Sensory Hearing Loss [NCIt concept]
- Sensory hearing loss (disorder) [SNOMED CT concept]
- Unspecified sensorineural hearing loss [ICD-10 Sub-category]
- sensorineural hearing loss [DO Concept]
- sensorineural hearing loss [Disease (Nov.)]
- sensorineural hearing loss, nos [SNOMED Notion]
DO Cross reference
- sensorineural hearing loss [DO Concept]
HPO term
- Sensorineural hearing impairment [HPO term]
Indexing information
- KCNQ4 protein, human [MeSH Supplementary Concept]
- Kcnq4 protein, mouse [MeSH Supplementary Concept]
- Kcnq4 protein, rat [MeSH Supplementary Concept]
- STRC protein, human [MeSH Supplementary Concept]
Record concept(s)
- hearing loss, cochlear [MeSH concept]
- hearing loss, sensorineural [MeSH concept]
Related MeSH Supplementary Concept(s)
- Axenfeld-Rieger anomaly with cardiac defects and sensorineural hearing loss [MeSH Supplementary Concept]
- Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities [MeSH Supplementary Concept]
- BADS syndrome [MeSH Supplementary Concept]
- Brown-Vialetto-Van laere syndrome [MeSH Supplementary Concept]
- CAPOS syndrome [MeSH Supplementary Concept]
- Charcot-Marie-Tooth disease and deafness [MeSH Supplementary Concept]
- Charcot-Marie-Tooth disease, type 2J [MeSH Supplementary Concept]
- Chudley-Mccullough syndrome [MeSH Supplementary Concept]
- Coloboma, cleft lip-palate and mental retardation syndrome [MeSH Supplementary Concept]
- Deafness, Autosomal Recessive 4 [MeSH Supplementary Concept]
- Donnai-Barrow syndrome [MeSH Supplementary Concept]
- HID syndrome [MeSH Supplementary Concept]
- Insulin-Like growth factor I deficiency [MeSH Supplementary Concept]
- MYH9-Related Disorders [MeSH Supplementary Concept]
- Martin-Probst Deafness-Mental retardation syndrome [MeSH Supplementary Concept]
- Otofacioosseous-Gonadal syndrome [MeSH Supplementary Concept]
- Palmoplantar Keratoderma with Deafness [MeSH Supplementary Concept]
- Rod-Cone dystrophy, sensorineural deafness, and Fanconi-Type renal dysfunction [MeSH Supplementary Concept]
- SeSAME syndrome [MeSH Supplementary Concept]
- Split-Hand-Foot Malformation With Sensorineural Hearing Loss [MeSH Supplementary Concept]
- Townes-Brocks syndrome [MeSH Supplementary Concept]
- Townes-Brocks-Branchiootorenal-Like syndrome [MeSH Supplementary Concept]
- acrootoocular syndrome [MeSH Supplementary Concept]
- albinism ocular late onset sensorineural deafness [MeSH Supplementary Concept]
- arthrogryposis-like hand anomaly and sensorineural deafness [MeSH Supplementary Concept]
- ataxia, deafness, and cardiomyopathy [MeSH Supplementary Concept]
- athabaskan brainstem dysgenesis [MeSH Supplementary Concept]
- atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus, photomyoclonus, and degenerative neurologic disease [MeSH Supplementary Concept]
- auditory neuropathy, nonsyndromic recessive [MeSH Supplementary Concept]
- barakat syndrome [MeSH Supplementary Concept]
- bartter syndrome, type 4A [MeSH Supplementary Concept]
- bartter syndrome, type 4b [MeSH Supplementary Concept]
- bjornstad syndrome [MeSH Supplementary Concept]
- boudhina yedes khiari syndrome [MeSH Supplementary Concept]
- brachydactyly, intraventricular septal defect, and deafness [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1J [MeSH Supplementary Concept]
- cataract ataxia deafness [MeSH Supplementary Concept]
- cataracts, congenital, with sensorineural deafness, down Syndrome-Like facial appearance, short stature, and mental retardation [MeSH Supplementary Concept]
- cerebellar ataxia and hypergonadotropic hypogonadism [MeSH Supplementary Concept]
- cerebellar ataxia and neurosensory deafness [MeSH Supplementary Concept]
- cerebellar ataxia, deafness, and narcolepsy [MeSH Supplementary Concept]
- chitty hall baraitser syndrome [MeSH Supplementary Concept]
- cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss [MeSH Supplementary Concept]
- cochleosaccular degeneration of the inner ear and progressive cataracts [MeSH Supplementary Concept]
- congenital ectodermal dysplasia with hearing loss [MeSH Supplementary Concept]
- corneal dystrophy and perceptive deafness [MeSH Supplementary Concept]
- cowchock syndrome [MeSH Supplementary Concept]
- craniofacial deafness hand syndrome [MeSH Supplementary Concept]
- cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness [MeSH Supplementary Concept]
- deafness enamel hypoplasia nail defects [MeSH Supplementary Concept]
- deafness oligodontia syndrome [MeSH Supplementary Concept]
- deafness, Aminoglycoside-Induced [MeSH Supplementary Concept]
- deafness, Childhood-Onset neurosensory, autosomal recessive 8 [MeSH Supplementary Concept]
- deafness, High-Frequency sensorineural, X-Linked [MeSH Supplementary Concept]
- deafness, Mid-Tone neural [MeSH Supplementary Concept]
- deafness, X-Linked 1 [MeSH Supplementary Concept]
- deafness, X-Linked 3 [MeSH Supplementary Concept]
- deafness, X-Linked 4 [MeSH Supplementary Concept]
- deafness, X-Linked 5 [MeSH Supplementary Concept]
- deafness, autosomal dominant 1 [MeSH Supplementary Concept]
- deafness, autosomal dominant 10 [MeSH Supplementary Concept]
- deafness, autosomal dominant 11 [MeSH Supplementary Concept]
- deafness, autosomal dominant 12 [MeSH Supplementary Concept]
- deafness, autosomal dominant 13 [MeSH Supplementary Concept]
- deafness, autosomal dominant 15 [MeSH Supplementary Concept]
- deafness, autosomal dominant 16 [MeSH Supplementary Concept]
- deafness, autosomal dominant 18 [MeSH Supplementary Concept]
- deafness, autosomal dominant 20 [MeSH Supplementary Concept]
- deafness, autosomal dominant 21 [MeSH Supplementary Concept]
- deafness, autosomal dominant 23 [MeSH Supplementary Concept]
- deafness, autosomal dominant 24 [MeSH Supplementary Concept]
- deafness, autosomal dominant 25 [MeSH Supplementary Concept]
- deafness, autosomal dominant 28 [MeSH Supplementary Concept]
- deafness, autosomal dominant 2A [MeSH Supplementary Concept]
- deafness, autosomal dominant 2B [MeSH Supplementary Concept]
- deafness, autosomal dominant 30 [MeSH Supplementary Concept]
- deafness, autosomal dominant 31 [MeSH Supplementary Concept]
- deafness, autosomal dominant 36 [MeSH Supplementary Concept]
- deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 [MeSH Supplementary Concept]
- deafness, autosomal dominant 3A [MeSH Supplementary Concept]
- deafness, autosomal dominant 3B [MeSH Supplementary Concept]
- deafness, autosomal dominant 4 [MeSH Supplementary Concept]
- deafness, autosomal dominant 41 [MeSH Supplementary Concept]
- deafness, autosomal dominant 43 [MeSH Supplementary Concept]
- deafness, autosomal dominant 44 [MeSH Supplementary Concept]
- deafness, autosomal dominant 47 [MeSH Supplementary Concept]
- deafness, autosomal dominant 48 [MeSH Supplementary Concept]
- deafness, autosomal dominant 49 [MeSH Supplementary Concept]
- deafness, autosomal dominant 5 [MeSH Supplementary Concept]
- deafness, autosomal dominant 52 [MeSH Supplementary Concept]
- deafness, autosomal dominant 53 [MeSH Supplementary Concept]
- deafness, autosomal dominant 59 [MeSH Supplementary Concept]
- deafness, autosomal dominant 6 [MeSH Supplementary Concept]
- deafness, autosomal dominant 7 [MeSH Supplementary Concept]
- deafness, autosomal dominant 9 [MeSH Supplementary Concept]
- deafness, autosomal dominant nonsyndromic sensorineural 17 [MeSH Supplementary Concept]
- deafness, autosomal dominant nonsyndromic sensorineural 22 [MeSH Supplementary Concept]
- deafness, autosomal dominant nonsyndromic sensorineural 23 [MeSH Supplementary Concept]
- deafness, autosomal dominant nonsyndromic sensorineural 24 [MeSH Supplementary Concept]
- deafness, autosomal recessive [MeSH Supplementary Concept]
- deafness, autosomal recessive 10 [MeSH Supplementary Concept]
- deafness, autosomal recessive 12 [MeSH Supplementary Concept]
- deafness, autosomal recessive 13 [MeSH Supplementary Concept]
- deafness, autosomal recessive 14 [MeSH Supplementary Concept]
- deafness, autosomal recessive 15 [MeSH Supplementary Concept]
- deafness, autosomal recessive 16 [MeSH Supplementary Concept]
- deafness, autosomal recessive 17 [MeSH Supplementary Concept]
- deafness, autosomal recessive 18 [MeSH Supplementary Concept]
- deafness, autosomal recessive 1A [MeSH Supplementary Concept]
- deafness, autosomal recessive 1b [MeSH Supplementary Concept]
- deafness, autosomal recessive 2 [MeSH Supplementary Concept]
- deafness, autosomal recessive 20 [MeSH Supplementary Concept]
- deafness, autosomal recessive 21 [MeSH Supplementary Concept]
- deafness, autosomal recessive 22 [MeSH Supplementary Concept]
- deafness, autosomal recessive 23 [MeSH Supplementary Concept]
- deafness, autosomal recessive 26 [MeSH Supplementary Concept]
- deafness, autosomal recessive 27 [MeSH Supplementary Concept]
- deafness, autosomal recessive 28 [MeSH Supplementary Concept]
- deafness, autosomal recessive 3 [MeSH Supplementary Concept]
- deafness, autosomal recessive 30 [MeSH Supplementary Concept]
- deafness, autosomal recessive 31 [MeSH Supplementary Concept]
- deafness, autosomal recessive 32 [MeSH Supplementary Concept]
- deafness, autosomal recessive 33 [MeSH Supplementary Concept]
- deafness, autosomal recessive 35 [MeSH Supplementary Concept]
- deafness, autosomal recessive 36 [MeSH Supplementary Concept]
- deafness, autosomal recessive 37 [MeSH Supplementary Concept]
- deafness, autosomal recessive 38 [MeSH Supplementary Concept]
- deafness, autosomal recessive 39 [MeSH Supplementary Concept]
- deafness, autosomal recessive 40 [MeSH Supplementary Concept]
- deafness, autosomal recessive 42 [MeSH Supplementary Concept]
- deafness, autosomal recessive 44 [MeSH Supplementary Concept]
- deafness, autosomal recessive 46 [MeSH Supplementary Concept]
- deafness, autosomal recessive 47 [MeSH Supplementary Concept]
- deafness, autosomal recessive 48 [MeSH Supplementary Concept]
- deafness, autosomal recessive 49 [MeSH Supplementary Concept]
- deafness, autosomal recessive 5 [MeSH Supplementary Concept]
- deafness, autosomal recessive 53 [MeSH Supplementary Concept]
- deafness, autosomal recessive 59 [MeSH Supplementary Concept]
- deafness, autosomal recessive 6 [MeSH Supplementary Concept]
- deafness, autosomal recessive 62 [MeSH Supplementary Concept]
- deafness, autosomal recessive 63 [MeSH Supplementary Concept]
- deafness, autosomal recessive 65 [MeSH Supplementary Concept]
- deafness, autosomal recessive 66 [MeSH Supplementary Concept]
- deafness, autosomal recessive 67 [MeSH Supplementary Concept]
- deafness, autosomal recessive 68 [MeSH Supplementary Concept]
- deafness, autosomal recessive 7 [MeSH Supplementary Concept]
- deafness, autosomal recessive 71 [MeSH Supplementary Concept]
- deafness, autosomal recessive 77 [MeSH Supplementary Concept]
- deafness, autosomal recessive 79 [MeSH Supplementary Concept]
- deafness, autosomal recessive 9 [MeSH Supplementary Concept]
- deafness, autosomal recessive, 24 [MeSH Supplementary Concept]
- deafness, congenital, with inner ear agenesis, microtia, and microdontia [MeSH Supplementary Concept]
- deafness, congenital, with total albinism [MeSH Supplementary Concept]
- deafness, progressive High-Tone neural [MeSH Supplementary Concept]
- deafness, sensorineural, Autosomal-Mitochondrial type [MeSH Supplementary Concept]
- deafness, sensorineural, and male infertility [MeSH Supplementary Concept]
- deafness, sensorineural, with hypertrophic cardiomyopathy [MeSH Supplementary Concept]
- deafness, sensorineural, with peripheral neuropathy and arterial disease [MeSH Supplementary Concept]
- digitorenocerebral syndrome [MeSH Supplementary Concept]
- ectodermal dysplasia and neurosensory deafness [MeSH Supplementary Concept]
- ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features [MeSH Supplementary Concept]
- ermine phenotype [MeSH Supplementary Concept]
- fitzsimmons walson mellor syndrome [MeSH Supplementary Concept]
- flynn aird syndrome [MeSH Supplementary Concept]
- friedreich ataxia, So-Called, with optic atrophy and sensorineural deafness [MeSH Supplementary Concept]
- gemignani syndrome [MeSH Supplementary Concept]
- gonadal dysgenesis XX type deafness [MeSH Supplementary Concept]
- griscelli syndrome type 1 [MeSH Supplementary Concept]
- histiocytosis with joint contractures and sensorineural deafness [MeSH Supplementary Concept]
- hittner hirsch kreh syndrome [MeSH Supplementary Concept]
- homozygous 11p15-p14 deletion syndrome [MeSH Supplementary Concept]
- johanson blizzard syndrome [MeSH Supplementary Concept]
- knuckle pads, leuconychia and sensorineural deafness [MeSH Supplementary Concept]
- lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones [MeSH Supplementary Concept]
- macrothrombocytopenia progressive deafness [MeSH Supplementary Concept]
- marshall syndrome [MeSH Supplementary Concept]
- nephropathy deafness hyperparathyroidism [MeSH Supplementary Concept]
- nephropathy with pretibial epidermolysis bullosa and deafness [MeSH Supplementary Concept]
- nephropathy, progressive, with deafness [MeSH Supplementary Concept]
- neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia [MeSH Supplementary Concept]
- nonsyndromic sensorineural hearing loss [MeSH Supplementary Concept]
- optic atrophy 1 and deafness [MeSH Supplementary Concept]
- optic atrophy, deafness, ophthalmoplegia, and myopathy [MeSH Supplementary Concept]
- otodental dysplasia [MeSH Supplementary Concept]
- paragangliomas with sensorineural hearing loss [MeSH Supplementary Concept]
- pendred syndrome [MeSH Supplementary Concept]
- pfeiffer kapferer syndrome [MeSH Supplementary Concept]
- progressive hearing loss stapes fixation [MeSH Supplementary Concept]
- prune belly syndrome with pulmonic stenosis, mental retardation, and deafness [MeSH Supplementary Concept]
- renal tubular acidosis, distal, autosomal recessive, with Late-Onset sensorineural hearing loss [MeSH Supplementary Concept]
- renal tubular acidosis, distal, with progressive nerve deafness [MeSH Supplementary Concept]
- retinitis pigmentosa inversa with deafness [MeSH Supplementary Concept]
- robinson miller bensimon syndrome [MeSH Supplementary Concept]
- schaap taylor baraitser syndrome [MeSH Supplementary Concept]
- sensorineural deafness with mild renal dysfunction [MeSH Supplementary Concept]
- sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth [MeSH Supplementary Concept]
- spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy [MeSH Supplementary Concept]
- spondyloepiphyseal dysplasia, myopia, and sensorineural deafness [MeSH Supplementary Concept]
- stickler syndrome, autosomal recessive, COL9A1-Related [MeSH Supplementary Concept]
- stickler syndrome, type 1 [MeSH Supplementary Concept]
- thiamine responsive megaloblastic anemia syndrome [MeSH Supplementary Concept]
- treft sanborn carey syndrome [MeSH Supplementary Concept]
- tunglang savage bellman syndrome [MeSH Supplementary Concept]
- vohwinkel syndrome [MeSH Supplementary Concept]
- winkelman bethge pfeiffer syndrome [MeSH Supplementary Concept]
- wolfram syndrome 2 [MeSH Supplementary Concept]
- wolfram syndrome, mitochondrial form [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Acquired sensorineural hearing loss [ICD-11 Subcategory]
- Deafness neurosensory [MedDRA Preferred Term]
- Neuro sensory deafness [MedDRA LLT]
- Perception hearing loss [PASCAL descriptor]
- Perceptive deafness [MedDRA LLT]
- Sensorineural Hearing Loss [NCIt concept]
- Sensorineural deafness [MedDRA LLT]
- Sensorineural deafness [HPO term]
- Sensorineural hearing impairment [HPO term]
- Sensorineural hearing loss [ICD-9 code]
- Sensorineural hearing loss [MedDRA LLT]
- Sensorineural hearing loss (disorder) [SNOMED CT concept]
- Sensorineural hearing loss, unspecified [MedDRA LLT]
- Sensorineural hearing loss, unspecified [ICD-9 code]
- Sensorineural hearing loss, unspecified [ICD-10 Sub-category (who)]
- Unspecified sensorineural hearing loss [ICD-10 Sub-category]
- sensorineural hearing loss [Disease (Nov.)]
- sensorineural hearing loss [DO Concept]
- sensorineural hearing loss, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- cochlear hearing loss [Disease (Nov.)]

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