AutoICD API

H90.5

Billable

Unspecified sensorineural hearing loss

Unspecified sensorineural hearing loss

Status

Billable / Specific

Block

H90-H94

Parent Code

H90

ICD-11 Mapping

1 equivalent

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

Related Codes(9)
H90.0

Conductive hearing loss, bilateral

BillableH90.1

Conductive hear loss, uni w unrestricted hear cntra side

H90.2

Conductive hearing loss, unspecified

BillableH90.3

Sensorineural hearing loss, bilateral

BillableH90.4

Sensorineural hear loss, uni w unrestricted hear cntra side

H90.6

Mixed conductive and sensorineural hearing loss, bilateral

BillableH90.7

Mixed cndct/snrl hear loss, uni w unrestr hear cntra side

H90.8

Mixed conductive and sensorineural hearing loss, unspecified

BillableH90.A

Cndct/snrl hearing loss with restricted hear cntra side

ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

AB51.ZAcquired hearing impairment, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(996)

SNOMED CT

UMLS

Clinical Terms

  • Cutaneous syndrome with ichthyosis
  • Congenital conductive hearing loss
  • Genetic syndromes of diabetes mellitus
  • Complete deafness
  • OPCA - Olivopontocerebellar atrophy
  • Steroid-resistant nephrotic syndrome
  • Congenital hereditary endothelial dystrophy and perceptive deafness syndrome
  • nerve conduction deafness
  • Progressive sensorineural deafness and hypertrophic cardiomyopathy syndrome
  • Asymmetrical sensorineural hearing loss
  • Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and deafness
  • Maternal perinatal sensorineural hearing loss
  • Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome
  • Micromelic dwarf
  • KIDS - Keratitis ichthyosis and deafness syndrome
  • Aproctia
  • Diabetes-deafness syndrome maternally transmitted
  • Ichthyosis hystrix Rheydt type
  • Sensory neuropathy
  • Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome
  • Essential tremor
  • Simmonds' disease
  • Deafness, pili torti, hypogonadism syndrome
  • Mandibular hypoplasia, deafness, progeroid syndrome
  • Selective tooth agenesis
  • Autosomal dominant KID (keratitis, ichthyosis, deafness) syndrome
  • Bilateral optic atrophy of eyes
  • CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
  • inner ear hearing loss
  • 3-methylglutaconic aciduria with hearing loss, encephalopathy, Leigh-like syndrome
  • Optic atrophy of both eyes
  • Asymmetric hearing loss
  • Sensorineural hearing loss of combined sites
  • Central hearing loss
  • Non-syndromic mitochondrial sensorineural deafness
  • Achalasia of cardia
  • Premature grayness of hair
  • Premature canities
  • Sensorineural hearing impairment
  • Deafness Neurosensory
  • Sensory hearing loss
  • Sensory hearing loss (disorder)
  • hearing loss sensorineural
  • CAPOS (cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss) syndrome
  • MEGDEL syndrome
  • Congenital hearing disorder
  • Craniofacial deafness hand syndrome
  • PD - Perceptive deafness
  • Hypogonadotropic hypogonadism, severe microcephaly, sensorineural deafness, dysmorphism syndrome
  • Hearing Loss, Central
  • Paroxysmal sleep
  • Hearing loss, pili torti, hypogonadism syndrome
  • Ocular albinism with late-onset sensorineural deafness
  • Deafness with malformation of ear and facial palsy syndrome
  • Macrodontia
  • Combined perceptive hearing loss
  • Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome
  • Sensorineural hearing loss, unspecified
  • Achalasia of oesophagus
  • Microcephaly with deafness and intellectual disability syndrome
  • Keratitis ichthyosis deafness syndrome
  • Congenital corneal dystrophy
  • Deafness-dystonia-optic neuronopathy syndrome
  • Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome
  • Retrocochlear Hearing Loss
  • High frequency sensorineural hearing loss
  • Progressive autosomal recessive ataxia, deafness syndrome
  • Arts syndrome
  • Keratitis, ichthyosis, deafness/hystrix-like ichthyosis deafness syndrome
  • Jones syndrome
  • Hereditary sensory neuropathy
  • Deafness-dystonia syndrome
  • HDR syndrome
  • Posterior sensory radicular neuropathy
  • Deafness and oligodontia syndrome
  • Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome
  • Hearing loss, perceptive
  • Maternally-inherited diabetes and hearing loss
  • Renal tubular acidosis with deafness
  • Colobomatous microphthalmia
  • Hypoparathyroidism, deafness, renal disease syndrome
  • Congenital kyphosis
  • Sensoryneural Deafnesses
  • Spinocerebellar ataxia, amyotrophy, deafness syndrome
  • Ehlers-Danlos syndrome type 6
  • Sellars Beighton syndrome
  • Stoll Lévy Francfort syndrome
  • Braun Bayer syndrome
  • Sensory-neural deafness
  • Sommer Young Wee Frye syndrome
  • Hereditary gingival fibromatosis
  • Congenital deafness
  • Hypertelorism, preauricular sinus, punctual pits, deafness syndrome
  • Congenital cataract, deafness, severe developmental delay syndrome
  • Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency
  • Liberfarb syndrome
  • Deafness and hypogonadism syndrome
  • Type I renal tubular acidosis
  • Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibers
  • Lethal neurodegenerative disorder due to copper transport defect
  • Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
  • Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome
  • Central deafness
  • Sensorineural Hearing Loss
  • Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
  • Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome
  • DOORS syndrome
  • COMMAD syndrome
  • Duane's retraction syndrome
  • Deafness, central
  • Pfeiffer Kapferer syndrome
  • Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
  • Benign neoplasm of sacrococcygeal region
  • Nephrotic syndrome, hearing loss, pretibial epidermolysis bullosa syndrome
  • KID/HID syndrome
  • Chromosome 15q15.3 deletion syndrome
  • Thong Douglas Ferrante syndrome
  • Congenital calyceal diverticulum
  • Deafness nerve type
  • Asymmetrical hearing loss
  • Gelineau's syndrome
  • Nanomelia
  • Premature graying
  • Deafness, congenital
  • Mandibular hypoplasia, hearing loss, progeroid syndrome
  • CHED-congenital hereditary endothelial dystrophy
  • Deafness, sensorineural
  • Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome
  • Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss
  • High tone sensorineural hearing loss
  • sensorineural deafness
  • Senter syndrome
  • Dejerine-Thomas syndrome
  • Deafness, encephaloneuropathy, obesity, valvulopathy syndrome
  • Bjornstad's syndrome
  • Orbital separation excessive
  • Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome
  • Hearing loss and salivary gland insensitivity to aldosterone syndrome
  • Marquardt-Loriaux syndrome
  • Albright's renal tubular acidosis
  • Barakat syndrome
  • Leber's amaurosis
  • 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
  • Olivopontocerebellar atrophy
  • Nathalie syndrome
  • Perceptive hearing loss
  • Duane's syndrome
  • COMMAD (coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness) syndrome
  • Gemignani syndrome
  • Autosomal dominant hearing loss, onychodystrophy syndrome
  • 3-methylglutaconic aciduria with deafness, encephalopathy, Leigh-like syndrome
  • Perceptive hearing loss NOS
  • 10p partial monosomy syndrome
  • Sensorineural deafness NOS
  • Schaap Taylor Baraitser syndrome
  • Multiple malformation syndrome, moderate short stature, facial with or without genital features
  • SCAR19 - spinocerebellar ataxia, autosomal recessive 19
  • Nephrosis, deafness, urinary tract, digital malformation syndrome
  • Thomas' syndrome
  • Deafness with onychodystrophy syndrome
  • Keipert syndrome
  • neural hearing loss
  • Congenital cataract, hearing loss, severe developmental delay syndrome
  • Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome
  • Gonadal dysgenesis with sensorineural deafness, autosomal recessive inheritance
  • KID syndrome
  • Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome
  • Wolfram syndrome type 1
  • Deafness, nephritis, anorectal malformation syndrome
  • perceptive deafness
  • Congenital cataract with deafness and hypogonadism syndrome
  • Sensorineural hearing loss of right ear
  • Deafness infertility syndrome
  • EAST (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome
  • DIAPH1-related sensorineural deafness, thrombocytopenia syndrome
  • Congenital atresia of anus
  • WFS2 - Wolfram syndrome-2
  • Cochlear hearing loss
  • Congenital nephritis
  • Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
  • Chitty Hall Baraitser syndrome
  • Neural hearing loss of left ear
  • Retinitis pigmentosa-deafness syndrome type 3
  • Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome
  • Wolfram syndrome
  • Deafness nerve
  • Cleft palate and cleft lip with deafness and sacral lipoma syndrome
  • Neural hearing loss of right ear
  • Sensorineural deafness and male infertility
  • Body height below reference range
  • Congenital retinal blindness
  • Hypertelorism
  • SNHL - Sensorineural hearing loss
  • Adult-onset progressive leucoencephalopathy, early-onset deafness
  • Central hearing loss (disorder)
  • Deafness, vitiligo, achalasia syndrome
  • Thiamine-responsive megaloblastic anaemia syndrome
  • Usher's syndrome
  • Ehlers-Danlos syndrome kyphoscoliotic and hearing loss type
  • Congenital sensorineural deafness
  • Sensory-neural hearing loss
  • hereditary deafness
  • Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome
  • Dead ear - postoperative
  • Acquired sensorineural hearing loss
  • Generalised dystonia
  • Lichtenstein Knorr syndrome
  • Congenital imperforate anus
  • Cardiospasm
  • Diverticulum of renal calyx
  • High frequency sensorineural hearing loss in right ear
  • Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
  • Leber congenital amaurosis
  • Central hearing loss NOS
  • Gingival fibromatosis with progressive deafness syndrome
  • Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome
  • nerve deafness
  • Keratitis ichthyosis and deafness syndrome
  • Renal tubular acidosis with progressive nerve deafness
  • Sensory hearing loss NOS
  • Sensoryneural Deafness
  • Neonatal sensorineural hearing loss
  • X-linked sensorineural hearing loss
  • Congenital achalasia of esophagus
  • Hypertelorism, preauricular sinus, punctual pits, hearing loss syndrome
  • Harboyan syndrome
  • Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome
  • Congenital osteodystrophy
  • Neurosensory deafness
  • Primary hypersomnia
  • Central auditory dysfunction
  • Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
  • Gingival fibromatosis
  • Low frequency sensorineural hearing loss
  • End organ deafness
  • Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
  • Duane retraction syndrome with congenital hearing loss
  • Premature greyness of hair
  • Retinitis pigmentosa, deafness, mental retardation, hypogonadism syndrome
  • Ehlers-Danlos syndrome kyphoscoliotic type
  • Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome
  • Perrault syndrome
  • Autosomal dominant deafness with onychodystrophy syndrome
  • Wolfram syndrome type I
  • Finucane Kurtz Scott syndrome
  • Hypotrichosis and deafness syndrome
  • Micromelus
  • Congenital preauricular fistula
  • Duane retraction syndrome
  • RTA (renal tubular acidosis) type I
  • Hereditary fibrous enlargement of gingiva
  • Björnstad syndrome
  • Peripheral neuropathy with sensorineural hearing impairment syndrome
  • Hearing loss, encephaloneuropathy, obesity, valvulopathy syndrome
  • Atresia ani
  • Distal renal tubular acidosis co-occurrent with sensorineural deafness
  • Profound hearing loss
  • Neurosensory Deafnesses
  • Corneal dystrophy with progressive deafness
  • Narcolepsy
  • Usher syndrome
  • Aphonia, deafness, retinal dystrophy, duplicated halluces, intellectual disability syndrome
  • Congenital hearing loss
  • Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome
  • WFS1 - Wolfram syndrome-1
  • Albinism with deafness syndrome
  • Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
  • Lack of reflex relaxation of lower oesophageal sphincter
  • MIDD - maternally inherited diabetes and deafness
  • Microcephaly, intellectual disability, sensorineural deafness, epilepsy, abnormal muscle tone syndrome
  • Renal caliceal diverticuli and deafness syndrome
  • Deafness congenital
  • Ballinger-Wallace syndrome
  • Congenital deafness NOS
  • Lowe Kohn Cohen syndrome
  • Postoperative profound sensorineural hearing loss
  • Corneal dystrophy and perceptive deafness syndrome
  • Eyes wide apart
  • neural deafness
  • Deafness, Neurosensory
  • Black locks, oculocutaneous albinism, AND deafness of the sensorineural type
  • Congenital megacolon
  • Hearing Loss, Retrocochlear
  • Congenital kyphoscoliosis
  • Hereditary essential tremor
  • sensorineural hearing losses
  • Classic distal renal tubular acidosis
  • Congenital sensorineural hearing loss
  • HDR (hypoparathyroidism, sensorineural deafness, renal disease) syndrome
  • Duane syndrome
  • DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, deafness) syndrome
  • Spondyloepiphyseal dysplasia MacDermot type
  • Megalodontia
  • Deafness craniofacial syndrome
  • Congenital pernicious anaemia
  • Asymmetric sensorineural hearing loss
  • Wolfram syndrome type 2
  • Adult-onset progressive leukoencephalopathy, early-onset hearing loss
  • Orbital hypertelorism
  • Globodontia
  • Calyceal diverticulum
  • Sudden hearing loss
  • SND - Sensorineural deafness
  • Dentinogenesis imperfecta
  • Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
  • Sensorineural hearing loss, early graying, essential tremor syndrome
  • Hearing loss, congenital
  • Wolfram syndrome type II
  • Deletion of part of chromosome 11
  • Autoimmune sensorineural hearing loss
  • Male infertility of chromosomal origin
  • 3-Methylglutaconic aciduria type 4
  • Severe X-linked intellectual disability Gustavson type
  • Congenital prelingual deafness
  • Fistula auris congenita
  • Sensorineural hearing loss in left ear
  • Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome
  • Congenital hunchback
  • DDOD (dominant deafness onychodystrophy) syndrome
  • Adult-onset progressive leucoencephalopathy, early-onset hearing loss
  • Congenital deafness (disorder)
  • Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
  • MDP (mandibular hypoplasia, deafness, progeroid) syndrome
  • Sensorineural deafness due to late congenital syphilis
  • Stilling-Turk-Duane syndrome
  • Olivopontocerebellar atrophy and deafness
  • Panhypopituitarism
  • Diabetes, hypogonadism, deafness, intellectual disability syndrome
  • Thiamine-responsive megaloblastic anemia
  • Heritable disorder of neutrophil function
  • PCNA-related progressive neurodegenerative photosensitivity syndrome
  • Preauricular fistula
  • Deafnesses, Sensoryneural
  • Neuro sensory deafness
  • Micromelia
  • Maternally inherited cardiomyopathy and hearing loss syndrome
  • Generalized dystonia
  • Premature greying
  • SRNS - Steroid-resistant nephrotic syndrome
  • Hearing impairment, sensorineural
  • Dominant sensorineural hearing loss
  • Santos Mateus Leal syndrome
  • Sensorineural hearing loss, early greying, essential tremor syndrome
  • HPPD (hypertelorism, preauricular sinus, punctual pits, deafness) syndrome
  • Duane syndrome, type 3
  • Megaloblastic anaemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
  • Deafness with epiphyseal dysplasia and short stature syndrome
  • Epiphyseal dysplasia, hearing loss, dysmorphism syndrome
  • Preauricular sinus
  • Autosomal recessive deafness onychodystrophy syndrome
  • Congenital pernicious anemia
  • Hereditary growth hormone deficiency
  • OA - Ocular albinism
  • Duane retraction syndrome with congenital deafness
  • Sinoatrial node dysfunction and deafness
  • Deafness with cataract and skeletal anomaly syndrome
  • Hearing Loss, Sensorineural
  • Recessive sensorineural hearing loss
  • Phocomelic dwarf
  • Olivopontocerebellar degeneration
  • Duane's syndrome, type 3
  • Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibres
  • Neuropathy with hearing impairment
  • Congenital absence of proximal portion of limb
  • Déjérine-Thomas syndrome
  • Retinitis pigmentosa-deafness syndrome
  • Neural hearing loss (disorder)
  • Multiple malformation syndrome, moderate short stature, facial
  • Syndromic sensorineural hearing loss due to COXPD (combined oxidative phosphorylation defect)
  • Congenital cataract with ataxia and deafness syndrome
  • Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome
  • Non-acquired combined pituitary hormone deficiency, deafness, rigid cervical spine syndrome
  • Oculootodental syndrome
  • Usher syndrome type 3
  • Congenital cataract, progressive muscular hypotonia, deafness, developmental delay syndrome
  • Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome
  • Congenital achalasia of oesophagus
  • Dead ear
  • Lethal ataxia-deafness-optic atrophy
  • Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome
  • Congenital atrophy of optic nerve
  • Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
  • Autosomal dominant keratitis, ichthyosis, deafness syndrome
  • Chronic deafness
  • Maternally inherited cardiomyopathy and deafness
  • Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome
  • Microphthalmia with colobomatous cyst
  • Deafness, Sensoryneural
  • Lipoma of lower back
  • Pili torti-deafness syndrome
  • Lack of reflex relaxation of lower esophageal sphincter
  • sensory neuro deafness
  • Olivocerebellar atrophy
  • Twisted hair
  • Diabetes mellitus associated with genetic syndrome
  • Deafnesses, Neurosensory
  • Congenital humpback
  • Postnatal acquired sensorineural hearing loss
  • Familial steroid-resistant nephrotic syndrome with sensorineural deafness
  • Low tone sensorineural hearing loss
  • Deletion of part of chromosome 10
  • DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome
  • SHILCA syndrome
  • Thiamine-responsive megaloblastic anaemia
  • CRB - Congenital retinal blindness
  • Megaloblastic anaemia due to inborn errors of metabolism
  • Oligodontia
  • Sudden sensorineural hearing loss
  • AR dRTA (autosomal recessive distal renal tubular acidosis) with deafness
  • Fatal X-linked ataxia with deafness and loss of vision
  • Sensorineural deafness with dilated cardiomyopathy syndrome
  • Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome
  • Megaloblastic anemia due to inborn errors of metabolism
  • Profound acquired hearing loss
  • Auditory synaptopathy
  • Simmond's disease
  • Syndromic sensorineural deafness due to COXPD (combined oxidative phosphorylation defect)
  • Ocular albinism
  • Thiamine-responsive megaloblastic anemia syndrome
  • Rogers syndrome
  • Megadontia
  • Optic atrophy of bilateral eyes
  • BADS syndrome
  • Adult-onset progressive leukoencephalopathy, early-onset deafness
  • SESAME syndrome
  • Distal renal tubular acidosis
  • Achalasia of esophagus
  • Developmental malformation, deafness, dystonia syndrome
  • Ectodermal dysplasia and sensorineural deafness syndrome
  • Eyes widely set
  • DOOR syndrome
  • Steroid-unresponsive nephrotic syndrome
  • Profound sensorineural hearing loss
  • Lowry Yong syndrome
  • Hereditary opalescent dentin
  • Imperforate anus
  • Deficient secretion of all pituitary hormones
  • Autosomal recessive keratitis-ichthyosis-deafness syndrome
  • Late congenital syphilitic sensorineural deafness
  • Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome
  • Hearing Loss, Cochlear
  • Maternally inherited diabetes and deafness
  • Sensorineural hearing loss in right ear
  • Narcoleptic syndrome
  • Autosomal recessive distal renal tubular acidosis with deafness
  • Sensorineural hearing loss (disorder)
  • Sensorineural hearing loss of left ear
  • Macrodontism
  • Leber amaurosis
  • Congenital optic atrophy
  • Neutropenia, monocytopenia, deafness syndrome
  • Phocomelia
  • Primary hypopituitarism
  • Tungland Bellman syndrome
  • Neural hearing loss NOS
  • Nasodigitoacoustic syndrome
  • Autosomal dominant myopia, midfacial retrusion, sensorineural deafness, rhizomelic dysplasia syndrome
  • Aphonia, hearing loss, retinal dystrophy, duplicated halluces, intellectual disability syndrome
  • Kawashima Tsuji syndrome
  • Mitochondrial diabetes
  • DIDMOAD syndrome
  • hearing loss sensori neural
  • Congenital hereditary endothelial dystrophy
  • Microphthalmos co-occurrent with congenital ocular coloboma
  • Anal atresia
  • Eye retraction syndrome
  • Ehlers-Danlos syndrome kyphoscoliotic and deafness type
  • Autosomal dominant ichthyosis
  • SESAME (seizures, sensorineural deafness, ataxia, mental retardation, electrolyte imbalance) syndrome
  • Cochlear nerve deafness
  • Congenital dystrophy of cornea
  • Hirschsprung disease with deafness and polydactyly syndrome
  • Woodhouse Sakati syndrome
  • Ehlers-Danlos syndrome type VI
  • Mohr-Tranebjaerg syndrome
  • Pili torti
  • Congenital dilatation of colon
Frequently Asked Questions
What is the ICD-10 code for unspecified sensorineural hearing loss?

The ICD-10-CM code for unspecified sensorineural hearing loss is H90.5. The full clinical description is "Unspecified sensorineural hearing loss". H90.5 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code H90.5 mean?

ICD-10-CM code H90.5 represents “Unspecified sensorineural hearing loss”. It is classified under Chapter 8: Diseases of the Ear and Mastoid Process and 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: 6002006, 297233004, 711409002, 236532003, 45564002, 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.

How does H90.5 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like unspecified sensorineural hearing loss affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of H90.5?

H90.5 maps to the ICD-11 code: AB51.Z (Acquired hearing impairment, unspecified).

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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.