H90.5
BillableUnspecified sensorineural hearing loss
Unspecified sensorineural hearing loss
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Central hearing loss NOS
- Congenital deafness NOS
- Neural hearing loss NOS
- Perceptive hearing loss NOS
- Sensorineural deafness NOS
- Sensory hearing loss NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- Autosomal dominant KID (keratitis, ichthyosis, deafness) syndrome2625009
- Autosomal dominant keratitis, ichthyosis, deafness syndrome2625009
- Senter syndrome2625009
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- 10p partial monosomy syndrome6002006
- Complete deafness8531006
- BADS syndrome10170007
- Black locks, oculocutaneous albinism, AND deafness of the sensorineural type10170007
- Hereditary sensory neuropathy11442006
- Posterior sensory radicular neuropathy11442006
- Thiamine-responsive megaloblastic anaemia12907000
- Thiamine-responsive megaloblastic anemia12907000
- Pili torti17170005
- Twisted hair17170005
- Eyes wide apart22006008
- Eyes widely set22006008
- Hypertelorism22006008
- Orbital hypertelorism22006008
- Orbital separation excessive22006008
- Congenital absence of proximal portion of limb22841008
- Phocomelia22841008
- Phocomelic dwarf22841008
- Congenital dilatation of colon24291004
- Congenital megacolon24291004
- OA - Ocular albinism26399002
- Ocular albinism26399002
- Deficient secretion of all pituitary hormones32390006
- Panhypopituitarism32390006
- Primary hypopituitarism32390006
- Simmond's disease32390006
- Simmonds' disease32390006
- Congenital pernicious anaemia34925000
- Congenital pernicious anemia34925000
- Megaloblastic anaemia due to inborn errors of metabolism34925000
- Megaloblastic anemia due to inborn errors of metabolism34925000
- Primary hypersomnia36124002
- Achalasia of cardia45564002
- Achalasia of esophagus45564002
- Achalasia of oesophagus45564002
- Cardiospasm45564002
- Lack of reflex relaxation of lower esophageal sphincter45564002
- Lack of reflex relaxation of lower oesophageal sphincter45564002
- End organ deafness56943007
- Retinitis pigmentosa-deafness syndrome57838006
- Usher syndrome57838006
- Usher's syndrome57838006
- Gingival fibromatosis58569000
- Duane retraction syndrome60318001
- Duane syndrome60318001
- Duane's retraction syndrome60318001
- Duane's syndrome60318001
- Eye retraction syndrome60318001
- Stilling-Turk-Duane syndrome60318001
- Gelineau's syndrome60380001
- Narcolepsy60380001
- Narcoleptic syndrome60380001
- Paroxysmal sleep60380001
- Neurosensory deafness60700002
- PD - Perceptive deafness60700002
- Perceptive deafness60700002
- Perceptive hearing loss60700002
- SND - Sensorineural deafness60700002
- SNHL - Sensorineural hearing loss60700002
- Sensorineural deafness60700002
- Sensorineural hearing loss60700002
- Sensory-neural deafness60700002
- Sensory-neural hearing loss60700002
- Sensorineural hearing loss of combined sites65680009
- Dejerine-Thomas syndrome67761004
- Déjérine-Thomas syndrome67761004
- OPCA - Olivopontocerebellar atrophy67761004
- Olivocerebellar atrophy67761004
- Olivopontocerebellar atrophy67761004
- Olivopontocerebellar degeneration67761004
- Thomas' syndrome67761004
- Bjornstad's syndrome67817003
- Björnstad syndrome67817003
- Deafness, pili torti, hypogonadism syndrome67817003
- Hearing loss, pili torti, hypogonadism syndrome67817003
- Pili torti-deafness syndrome67817003
- Central auditory dysfunction68467004
- Central deafness68467004
- Central hearing loss68467004
- DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, deafness) syndrome70694009
- DIDMOAD syndrome70694009
- Marquardt-Loriaux syndrome70694009
- Wolfram syndrome70694009
- Congenital humpback71311003
- Congenital hunchback71311003
- Congenital kyphosis71311003
- Macrodontia71485000
- Macrodontism71485000
- Megadontia71485000
- Megalodontia71485000
- Nerve conduction deafness73371001
- Nerve deafness73371001
- Neural hearing loss73371001
- Retrocochlear hearing loss73371001
- Micromelia74370006
- Micromelic dwarf74370006
- Micromelus74370006
- Nanomelia74370006
- Multiple malformation syndrome, moderate short stature, facial77701002
- Multiple malformation syndrome, moderate short stature, facial with or without genital features77701002
- Sudden hearing loss79471008
- Cochlear hearing loss85571008
- Inner ear hearing loss85571008
- Sensory hearing loss85571008
- Benign neoplasm of sacrococcygeal region92331005
- Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance93466004
- Gonadal dysgenesis with sensorineural deafness, autosomal recessive inheritance93466004
- Perrault syndrome93466004
- Sensory neuropathy95662005
- Congenital hearing disorder95827002
- Congenital deafness95828007
- Hereditary fibrous enlargement of gingiva109620006
- Hereditary gingival fibromatosis109620006
- Duane syndrome, type 3128084001
- Duane's syndrome, type 3128084001
- CRB - Congenital retinal blindness193413001
- Congenital retinal blindness193413001
- Leber amaurosis193413001
- Leber congenital amaurosis193413001
- Leber's amaurosis193413001
- Combined perceptive hearing loss194426007
- Dentinogenesis imperfecta196286005
- Hereditary opalescent dentin196286005
- Congenital preauricular fistula204272007
- Fistula auris congenita204272007
- Preauricular fistula204272007
- Preauricular sinus204272007
- Anal atresia204712000
- Aproctia204712000
- Atresia ani204712000
- Congenital atresia of anus204712000
- Congenital imperforate anus204712000
- Imperforate anus204712000
- Chronic deafness232325008
- Dominant sensorineural hearing loss232328005
- X-linked sensorineural hearing loss232329002
- Recessive sensorineural hearing loss232330007
- Postnatal acquired sensorineural hearing loss232332004
- SRNS - Steroid-resistant nephrotic syndrome236381000
- Steroid-resistant nephrotic syndrome236381000
- Steroid-unresponsive nephrotic syndrome236381000
- Albright's renal tubular acidosis236461000
- Classic distal renal tubular acidosis236461000
- Distal renal tubular acidosis236461000
- RTA (renal tubular acidosis) type I236461000
- Type I renal tubular acidosis236461000
- AR dRTA (autosomal recessive distal renal tubular acidosis) with deafness236532003
- Autosomal recessive distal renal tubular acidosis with deafness236532003
- Renal tubular acidosis with deafness236532003
- Renal tubular acidosis with progressive nerve deafness236532003
- Male infertility of chromosomal origin236791009
- Megaloblastic anaemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness237617006
- Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness237617006
- Rogers syndrome237617006
- Thiamine-responsive megaloblastic anaemia syndrome237617006
- Thiamine-responsive megaloblastic anemia syndrome237617006
- Ballinger-Wallace syndrome237619009
- Diabetes-deafness syndrome maternally transmitted237619009
- MIDD - maternally inherited diabetes and deafness237619009
- Maternally inherited diabetes and deafness237619009
- Maternally-inherited diabetes and hearing loss237619009
- Mitochondrial diabetes237619009
- Cutaneous syndrome with ichthyosis239057002
- KID syndrome239059004
- Ichthyosis hystrix Rheydt type239059004
- KID/HID syndrome239059004
- KIDS - Keratitis ichthyosis and deafness syndrome239059004
- Keratitis ichthyosis and deafness syndrome239059004
- Keratitis ichthyosis deafness syndrome239059004
- Keratitis, ichthyosis, deafness/hystrix-like ichthyosis deafness syndrome239059004
- Congenital calyceal diverticulum253875000
- Congenital nephritis276585000
- Dead ear - postoperative277424008
- Postoperative profound sensorineural hearing loss277424008
- 3-Methylglutaconic aciduria type 4297233004
- Lipoma of lower back307754008
- Premature canities387833009
- Premature graying387833009
- Premature grayness of hair387833009
- Premature greying387833009
- Premature greyness of hair387833009
- Autosomal dominant ichthyosis402770002
- Heritable disorder of neutrophil function402794002
- Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome403780007
- Autosomal recessive keratitis-ichthyosis-deafness syndrome403780007
- Congenital kyphoscoliosis405772002
- CHED-congenital hereditary endothelial dystrophy417651000
- Congenital hereditary endothelial dystrophy417651000
- Generalised dystonia425492002
- Generalized dystonia425492002
- Asymmetric hearing loss427772009
- Asymmetrical hearing loss427772009
- Autoimmune sensorineural hearing loss428470000
- Asymmetric sensorineural hearing loss428887009
- Asymmetrical sensorineural hearing loss428887009
- Calyceal diverticulum433036004
- Diverticulum of renal calyx433036004
- Acquired sensorineural hearing loss609125008
- Essential tremor609558009
- Hereditary essential tremor609559001
- Congenital prelingual deafness699238006
- Congenital achalasia of esophagus700283004
- Congenital achalasia of oesophagus700283004
- Congenital sensorineural deafness700453005
- Congenital sensorineural hearing loss700453005
- Dead ear700454004
- Profound sensorineural hearing loss700454004
- Chromosome 15q15.3 deletion syndrome700489002
- Deafness infertility syndrome700489002
- Sensorineural deafness and male infertility700489002
- Craniofacial deafness hand syndrome702362004
- Sommer Young Wee Frye syndrome702362004
- Deafness-dystonia syndrome702423009
- Deafness-dystonia-optic neuronopathy syndrome702423009
- Mohr-Tranebjaerg syndrome702423009
- Arts syndrome702441001
- Fatal X-linked ataxia with deafness and loss of vision702441001
- Lethal ataxia-deafness-optic atrophy702441001
- Globodontia707310009
- 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome711409002
- 3-methylglutaconic aciduria with deafness, encephalopathy, Leigh-like syndrome711409002
- 3-methylglutaconic aciduria with hearing loss, encephalopathy, Leigh-like syndrome711409002
- MEGDEL syndrome711409002
- Sudden sensorineural hearing loss715239002
- Olivopontocerebellar atrophy and deafness715483009
- Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss715483009
- Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome715506001
- Stoll Lévy Francfort syndrome715506001
- Deafness and oligodontia syndrome715527006
- Colobomatous microphthalmia715771008
- Microphthalmia with colobomatous cyst715771008
- Microphthalmos co-occurrent with congenital ocular coloboma715771008
- Cleft palate and cleft lip with deafness and sacral lipoma syndrome716007007
- Lowry Yong syndrome716007007
- Kawashima Tsuji syndrome716112005
- Microcephaly with deafness and intellectual disability syndrome716112005
- Deafness with cataract and skeletal anomaly syndrome716170005
- Nathalie syndrome716170005
- Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome716192009
- Thong Douglas Ferrante syndrome716192009
- Chitty Hall Baraitser syndrome716238003
- Deafness with epiphyseal dysplasia and short stature syndrome716238003
- Hearing loss and salivary gland insensitivity to aldosterone syndrome716239006
- Tungland Bellman syndrome716239006
- Deafness with malformation of ear and facial palsy syndrome716243005
- Sellars Beighton syndrome716243005
- Deafness craniofacial syndrome716245003
- Ehlers-Danlos syndrome kyphoscoliotic type718211004
- Ehlers-Danlos syndrome type 6718211004
- Ehlers-Danlos syndrome type VI718211004
- Deafness and hypogonadism syndrome718714006
- Spondyloepiphyseal dysplasia MacDermot type718763005
- Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome718763005
- Congenital cataract with ataxia and deafness syndrome719102004
- Progressive sensorineural deafness and hypertrophic cardiomyopathy syndrome719272007
- Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome719272007
- Autosomal recessive deafness onychodystrophy syndrome719800009
- DOOR syndrome719800009
- DOORS syndrome719800009
- Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome719800009
- CAPOS (cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss) syndrome720634003
- Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome720634003
- Congenital hereditary endothelial dystrophy and perceptive deafness syndrome720749004
- Corneal dystrophy and perceptive deafness syndrome720749004
- Corneal dystrophy with progressive deafness720749004
- Harboyan syndrome720749004
- Ehlers-Danlos syndrome kyphoscoliotic and deafness type720859009
- Ehlers-Danlos syndrome kyphoscoliotic and hearing loss type720859009
- Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and deafness720859009
- Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency720859009
- Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome721086004
- Pfeiffer Kapferer syndrome721086004
- Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome721089006
- Developmental malformation, deafness, dystonia syndrome721092005
- EAST (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome721207002
- SESAME (seizures, sensorineural deafness, ataxia, mental retardation, electrolyte imbalance) syndrome721207002
- SESAME syndrome721207002
- Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome721207002
- Hirschsprung disease with deafness and polydactyly syndrome721221000
- Santos Mateus Leal syndrome721221000
- Ocular albinism with late-onset sensorineural deafness722054007
- Severe X-linked intellectual disability Gustavson type722213009
- Albinism with deafness syndrome722285005
- Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome722293005
- Congenital cataract with deafness and hypogonadism syndrome722378009
- Schaap Taylor Baraitser syndrome722378009
- Gingival fibromatosis with progressive deafness syndrome722449007
- Jones syndrome722449007
- Distal renal tubular acidosis co-occurrent with sensorineural deafness722468005
- Congenital atrophy of optic nerve722990003
- Congenital optic atrophy722990003
- Neuropathy with hearing impairment723497003
- Peripheral neuropathy with sensorineural hearing impairment syndrome723497003
- Sensorineural hearing loss, early graying, essential tremor syndrome723721007
- Sensorineural hearing loss, early greying, essential tremor syndrome723721007
- Sensorineural deafness with dilated cardiomyopathy syndrome723993005
- Retinitis pigmentosa, deafness, mental retardation, hypogonadism syndrome724001005
- Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome724001005
- Braun Bayer syndrome724092009
- Nephrosis, deafness, urinary tract, digital malformation syndrome724092009
- Maternally inherited cardiomyopathy and deafness724173009
- Maternally inherited cardiomyopathy and hearing loss syndrome724173009
- Barakat syndrome724282009
- HDR (hypoparathyroidism, sensorineural deafness, renal disease) syndrome724282009
- HDR syndrome724282009
- Hypoparathyroidism, deafness, renal disease syndrome724282009
- Neutropenia, monocytopenia, deafness syndrome725137007
- Deletion of part of chromosome 10726380001
- Deletion of part of chromosome 11726381002
- Ectodermal dysplasia and sensorineural deafness syndrome732953008
- Deafness, vitiligo, achalasia syndrome733069009
- Profound acquired hearing loss737050003
- Congenital conductive hearing loss737344003
- Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome763136000
- Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibers763136000
- Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibres763136000
- Deafness, encephaloneuropathy, obesity, valvulopathy syndrome763688008
- Hearing loss, encephaloneuropathy, obesity, valvulopathy syndrome763688008
- Keipert syndrome763774001
- Nasodigitoacoustic syndrome763774001
- Deafness, nephritis, anorectal malformation syndrome766249007
- Lowe Kohn Cohen syndrome766249007
- Epiphyseal dysplasia, hearing loss, dysmorphism syndrome766870005
- Finucane Kurtz Scott syndrome766870005
- Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome770751003
- Sinoatrial node dysfunction and deafness770784003
- Oculootodental syndrome770944002
- Non-acquired combined pituitary hormone deficiency, deafness, rigid cervical spine syndrome771308008
- Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome771308008
- Congenital cataract, progressive muscular hypotonia, deafness, developmental delay syndrome773398005
- Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome773398005
- MDP (mandibular hypoplasia, deafness, progeroid) syndrome773406003
- Mandibular hypoplasia, deafness, progeroid syndrome773406003
- Mandibular hypoplasia, hearing loss, progeroid syndrome773406003
- Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome773583007
- Aphonia, deafness, retinal dystrophy, duplicated halluces, intellectual disability syndrome773583007
- Aphonia, hearing loss, retinal dystrophy, duplicated halluces, intellectual disability syndrome773583007
- Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome773647007
- Nephrotic syndrome, hearing loss, pretibial epidermolysis bullosa syndrome773647007
- Congenital cataract, deafness, severe developmental delay syndrome773648002
- Congenital cataract, hearing loss, severe developmental delay syndrome773648002
- Lethal neurodegenerative disorder due to copper transport defect773648002
- Hypogonadotropic hypogonadism, severe microcephaly, sensorineural deafness, dysmorphism syndrome773665006
- Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome773665006
- HPPD (hypertelorism, preauricular sinus, punctual pits, deafness) syndrome773667003
- Hypertelorism, preauricular sinus, punctual pits, deafness syndrome773667003
- Hypertelorism, preauricular sinus, punctual pits, hearing loss syndrome773667003
- Deafness with onychodystrophy syndrome773735007
- Gemignani syndrome782690007
- Spinocerebellar ataxia, amyotrophy, deafness syndrome782690007
- Renal caliceal diverticuli and deafness syndrome782942003
- Hypotrichosis and deafness syndrome783555001
- Familial steroid-resistant nephrotic syndrome with sensorineural deafness783614008
- Oligodontia787414001
- Selective tooth agenesis787414001
- Auditory synaptopathy788873009
- Diabetes, hypogonadism, deafness, intellectual disability syndrome816067005
- Woodhouse Sakati syndrome816067005
- Congenital corneal dystrophy1003408005
- Congenital dystrophy of cornea1003408005
- Neural hearing loss of left ear1010229008
- Neural hearing loss of right ear1010230003
- Retinitis pigmentosa-deafness syndrome type 31010610007
- Usher syndrome type 31010610007
- Sensorineural hearing loss of right ear1119386008
- Sensorineural hearing loss of left ear1119387004
- Late congenital syphilitic sensorineural deafness1142112002
- Sensorineural deafness due to late congenital syphilis1142112002
- DIAPH1-related sensorineural deafness, thrombocytopenia syndrome1172604004
- DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome1172604004
- Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome1172604004
- Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome1172605003
- Maternal perinatal sensorineural hearing loss1179361001
- Neonatal sensorineural hearing loss1179362008
- Hereditary growth hormone deficiency1186807002
- Non-syndromic mitochondrial sensorineural deafness1187512003
- Autosomal dominant deafness with onychodystrophy syndrome1208614008
- Autosomal dominant hearing loss, onychodystrophy syndrome1208614008
- DDOD (dominant deafness onychodystrophy) syndrome1208614008
- CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome1220595008
- Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome1220595008
- PCNA-related progressive neurodegenerative photosensitivity syndrome1228871002
- Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome1228871002
- Autosomal dominant myopia, midfacial retrusion, sensorineural deafness, rhizomelic dysplasia syndrome1229999001
- Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome1229999001
- Duane retraction syndrome with congenital deafness1230014007
- Duane retraction syndrome with congenital hearing loss1230014007
- Profound hearing loss1230412003
- Lichtenstein Knorr syndrome1237413006
- Progressive autosomal recessive ataxia, deafness syndrome1237413006
- Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome1237413006
- SCAR19 - spinocerebellar ataxia, autosomal recessive 191237413006
- Microcephaly, intellectual disability, sensorineural deafness, epilepsy, abnormal muscle tone syndrome1254651003
- Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome1254651003
- Syndromic sensorineural deafness due to COXPD (combined oxidative phosphorylation defect)1260133007
- Syndromic sensorineural deafness due to combined oxidative phosphorylation defect1260133007
- Syndromic sensorineural hearing loss due to COXPD (combined oxidative phosphorylation defect)1260133007
- High frequency sensorineural hearing loss1268415009
- High tone sensorineural hearing loss1268415009
- Low frequency sensorineural hearing loss1268466004
- Low tone sensorineural hearing loss1268466004
- Liberfarb syndrome1284851009
- Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome1284851009
- WFS1 - Wolfram syndrome-11285518004
- Wolfram syndrome type 11285518004
- Wolfram syndrome type I1285518004
- WFS2 - Wolfram syndrome-21285519007
- Wolfram syndrome type 21285519007
- Wolfram syndrome type II1285519007
- Adult-onset progressive leucoencephalopathy, early-onset deafness1299152003
- Adult-onset progressive leucoencephalopathy, early-onset hearing loss1299152003
- Adult-onset progressive leukoencephalopathy, early-onset deafness1299152003
- Adult-onset progressive leukoencephalopathy, early-onset hearing loss1299152003
- COMMAD (coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness) syndrome1332382002
- COMMAD syndrome1332382002
- Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome1332382002
- SHILCA syndrome1356736002
- Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome1356736002
- Body height below reference range1363478003
- Bilateral optic atrophy of eyes15632891000119109
- Optic atrophy of bilateral eyes15632891000119109
- Optic atrophy of both eyes15632891000119109
- Congenital osteodystrophy5731000119108
- High frequency sensorineural hearing loss in right ear1091541000119108
- Sensorineural hearing loss in left ear23631000119109
- Sensorineural hearing loss in right ear23641000119100
UMLS
- Central Hearing LossC0018776
- Central deafnessC0018776
- Central hearing lossC0018776
- Central hearing loss (disorder)C0018776
- Central hearing loss NOSC0018776
- Deafness, centralC0018776
- Hearing Loss, CentralC0018776
- central hearing lossC0018776
- Cochlear Hearing LossC1691779
- Cochlear hearing lossC1691779
- Hearing Loss, CochlearC1691779
- Inner ear hearing lossC1691779
- Sensory Hearing LossC1691779
- Sensory hearing lossC1691779
- Sensory hearing loss (disorder)C1691779
- Sensory hearing loss NOSC1691779
- Cochlear nerve deafnessC0155550
- Deafness nerveC0155550
- Deafness nerve typeC0155550
- Hearing Loss, RetrocochlearC0155550
- Nerve conduction deafnessC0155550
- Nerve deafnessC0155550
- Neural deafnessC0155550
- Neural hearing lossC0155550
- Neural hearing loss (disorder)C0155550
- Neural hearing loss NOSC0155550
- Retrocochlear Hearing LossC0155550
- Retrocochlear hearing lossC0155550
- nerve conduction deafnessC0155550
- nerve deafnessC0155550
- neural deafnessC0155550
- neural hearing lossC0155550
- Congenital deafnessC0339789
- Congenital deafness (disorder)C0339789
- Congenital deafness NOSC0339789
- Congenital hearing lossC0339789
- Deafness congenitalC0339789
- Deafness, congenitalC0339789
- Hearing loss, congenitalC0339789
- Hereditary deafnessC0339789
- congenital deafnessC0339789
- congenital hearing lossC0339789
- hereditary deafnessC0339789
- Deafness NeurosensoryC0018784
- Deafness, NeurosensoryC0018784
- Deafness, SensoryneuralC0018784
- Deafness, sensorineuralC0018784
- Deafnesses, NeurosensoryC0018784
- Deafnesses, SensoryneuralC0018784
- Hearing Loss, SensorineuralC0018784
- Hearing impairment, sensorineuralC0018784
- Hearing loss, perceptiveC0018784
- Hearing loss, sensorineuralC0018784
- Neuro sensory deafnessC0018784
- Neurosensory DeafnessC0018784
- Neurosensory DeafnessesC0018784
- Neurosensory deafnessC0018784
- PD - Perceptive deafnessC0018784
- Perceptive deafnessC0018784
- Perceptive hearing lossC0018784
- Perceptive hearing loss NOSC0018784
- SND - Sensorineural deafnessC0018784
- SNHL - Sensorineural hearing lossC0018784
- Sensorineural DeafnessC0018784
- Sensorineural Hearing LossC0018784
- Sensorineural deafnessC0018784
- Sensorineural deafness NOSC0018784
- Sensorineural hearing impairmentC0018784
- Sensorineural hearing lossC0018784
- Sensorineural hearing loss (disorder)C0018784
- Sensorineural hearing loss, unspecifiedC0018784
- Sensory-neural deafnessC0018784
- Sensory-neural hearing lossC0018784
- Sensoryneural DeafnessC0018784
- Sensoryneural DeafnessesC0018784
- Unspecified sensorineural hearing lossC0018784
- hearing loss sensori neuralC0018784
- hearing loss sensorineuralC0018784
- inner ear hearing lossC0018784
- perceptive deafnessC0018784
- sensorineural deafnessC0018784
- sensorineural hearing lossC0018784
- sensorineural hearing lossesC0018784
- sensory hearing lossC0018784
- sensory neuro deafnessC0018784
Frequently Asked Questions
What is ICD-10 code H90.5?
ICD-10-CM code H90.5 represents "Unspecified sensorineural hearing loss". It is a billable/specific code that can be used on a claim.
Is H90.5 a billable code?
Yes, H90.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H90.5 in?
H90.5 is in Chapter 8: Diseases of the Ear and Mastoid Process (codes H60-H95).
What codes cannot be used with H90.5?
H90.5 has Excludes1 notes indicating codes that cannot be used together with it, including: deaf nonspeaking NEC (H91.3); deafness NOS (H91.9-); hearing loss NOS (H91.9-); and 5 more.
What SNOMED CT codes does H90.5 map to?
H90.5 maps to 197 SNOMED CT concepts: 239059004, 6002006, 297233004, 711409002, 236532003, and 192 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H90.5?
H90.5 is linked to 5 UMLS Concept Unique Identifiers: C0018776, C1691779, C0155550, C0339789, C0018784. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.