H91.90
BillableUnspecified hearing loss, unspecified ear
Unspecified hearing loss, unspecified ear
Coding Notes
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
- Bart-Pumphrey syndrome1271009
- Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome1271009
- Mixed sensory-motor polyneuropathy3900008
- Prune belly syndrome5187006
- Triad syndrome5187006
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- Congenital keratoderma6874009
- Complete deafness8531006
- Parathyroid hyperplasia9092004
- Hereditary sensory neuropathy11442006
- Posterior sensory radicular neuropathy11442006
- Congenital cleft hand13624003
- Lobster claw hand13624003
- Lobster-claw hand13624003
- Sensory polyneuropathy13694005
- Difficulty hearing15188001
- HI - Hearing impairment15188001
- HL - Hearing loss15188001
- HOH - Hard of hearing15188001
- Hard of hearing15188001
- Hearing impaired15188001
- Hearing impairment15188001
- Hearing loss15188001
- Hypoacusis15188001
- Impaired hearing15188001
- Garrod's pads16687001
- Knuckle pads16687001
- Congenital small ears35045004
- Microtia35045004
- Primary hyperparathyroidism36348003
- Congenital absence of abdominal muscle42190000
- Congenital leuconychia47139007
- Congenital leukonychia47139007
- Congenital anomaly of subcutaneous tissue56759000
- Retinitis pigmentosa-deafness syndrome57838006
- Usher syndrome57838006
- Usher's syndrome57838006
- DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, deafness) syndrome70694009
- DIDMOAD syndrome70694009
- Marquardt-Loriaux syndrome70694009
- Wolfram syndrome70694009
- Traumatic deafness, non-occupational72964008
- Hallgren's syndrome73119000
- Retinitis pigmentosa-deafness-ataxia syndrome73119000
- Nerve conduction deafness73371001
- Nerve deafness73371001
- Neural hearing loss73371001
- Retrocochlear hearing loss73371001
- Hereditary choroidal atrophy74469006
- Hereditary choroidal dystrophy74469006
- Choroideraemia75241009
- Choroideremia75241009
- Tapetochoroidal dystrophy75241009
- MHL - Mixed hearing loss77507001
- Mixed conductive AND sensorineural hearing loss77507001
- Mixed conductive and sensorineural deafness77507001
- Mixed deafness77507001
- Mixed hearing loss77507001
- Mixed type deafness77507001
- Motor polyneuropathy85423005
- Dominant autosomal hereditary disorder, incomplete penetrance87006007
- Traumatic deafness89496002
- Congenital anomaly of caudal vertebra92998007
- Sensory neuropathy95662005
- Bilateral hearing loss95820000
- Neonatal hearing loss95821001
- Decreased hearing103276001
- Auditory alteration128540005
- Disorder of hearing128540005
- Hearing disorder128540005
- Hearing difficulty162340000
- Rubella deafness186570004
- Conductive hearing loss, bilateral194417009
- Sensorineural hearing loss of bilateral ears194424005
- Sensorineural hearing loss of both ears194424005
- Mixed conductive and sensorineural hearing loss, bilateral194429000
- Atresia of posterior nares204508009
- Atresia of posterior naris204508009
- Choanal atresia204508009
- Congenital atresia of choana204508009
- Congenital atresia of posterior nares204508009
- Split foot205358006
- Cleft foot205358006
- Lobster claw foot205358006
- Deaf sounding voice229643008
- Voice associated with deafness229643008
- Voice associated with hearing loss229643008
- Usher syndrome type 1232057003
- Usher syndrome type 2232058008
- Chronic deafness232325008
- X-linked sensorineural hearing loss232329002
- Hearing loss associated with syndrome232333009
- Syndromal deafness232333009
- Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness236529001
- Prune belly syndrome with pulmonic stenosis, mental retardation and deafness236529001
- Herrmann syndrome237612000
- Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction237612000
- Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia239010003
- Finding of ability to hear whisper247301006
- Hearing for quiet voice247301006
- Hearing for whisper247301006
- Observation of ability to hear whisper247301006
- Finding of ability to hear loud voice247303009
- Hearing for loud voice247303009
- Observation of ability to hear loud voice247303009
- Otospondylomegaepiphyseal dysplasia254060000
- Disorder of speech and language development268672004
- Beradinelli-Seip syndrome284449005
- Berardinelli's syndrome284449005
- Berardinelli-Seip congenital lipodystrophy284449005
- Congenital generalised lipodystrophy284449005
- Congenital generalized lipodystrophy284449005
- Congenital total lipodystrophy284449005
- Lawrence-Seip syndrome284449005
- Lipoatrophic diabetes mellitus284449005
- Seip's syndrome284449005
- Total lipoatrophy284449005
- Finding of type of voice production289187009
- Observation of type of voice production289187009
- Hearing for conversational voice impaired300223008
- Hearing for loud voice impaired300225001
- Hearing for voice impaired300227009
- Hearing problem300228004
- Unable to hear whisper306970008
- Unable to hear conversational voice306971007
- Unable to hear loud voice306972000
- Spastic paraparesis312444006
- Partial deafness343087000
- Finding of ability to hear conversational voice399021008
- Hearing for conversational voice399021008
- Asymmetric hearing loss427772009
- Asymmetrical hearing loss427772009
- Combined visual and hearing impairment433147009
- Dual sensory impairment of vision and hearing433147009
- Speech and language developmental delay due to hearing loss441719005
- Speech, language developmental delay from hearing loss441719005
- Spastic paraparesis and deafness715504003
- Spastic paraparesis co-occurrent with deafness715504003
- Wells Jankovic syndrome715504003
- Ayazi syndrome717761005
- Choroideraemia with deafness and obesity syndrome717761005
- Choroideremia with deafness and obesity syndrome717761005
- Xq21 microdeletion syndrome717761005
- HSAN (hereditary sensory and autonomic neuropathy) with deafness and global delay717826009
- Hereditary sensory and autonomic neuropathy with deafness and global delay717826009
- Bilateral microtia with deafness and cleft palate syndrome717909004
- Abruzzo Erickson syndrome718574003
- CHARGE-like syndrome718574003
- Cleft palate with coloboma of eye and deafness syndrome718574003
- X-linked HSAN (hereditary sensory and autonomic neuropathy) with deafness719838008
- X-linked auditory neuropathy with peripheral sensory neuropathy type 1719838008
- X-linked hereditary sensory and autonomic neuropathy with deafness719838008
- Deafness and myopia syndrome720506002
- High myopia and sensorineural deafness720506002
- Ataxia with deafness and intellectual disability syndrome720517001
- Reardon Baraitser syndrome720517001
- Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome720519003
- Feigenbaum Bergeron Richardson syndrome720519003
- CATSHL (camptodactyly, tall stature, scoliosis, hearing loss) syndrome720601000
- Camptodactyly and tall stature with scoliosis and hearing loss syndrome720601000
- Burn McKeown syndrome720640005
- Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome720640005
- Deafness with skeletal dysplasia and lip granuloma syndrome720957007
- Deafness, skeletal dysplasia, coarse face with full lips syndrome720957007
- Fountain syndrome720957007
- Deaf blind hypopigmentation syndrome Yemenite type721084001
- Warburg Thomsen syndrome721084001
- Deafness, enamel hypoplasia, nail defect syndrome721085000
- Heimler syndrome721085000
- Deafness and intellectual disability Martin Probst type syndrome721087008
- Martin Probst syndrome721087008
- X-linked deafness and intellectual disability syndrome721087008
- Acquired hearing impairment721294001
- Acquired hearing loss721294001
- Lipodystrophy, intellectual disability, deafness syndrome721973006
- Rajab Spranger syndrome721973006
- IVIC (Instituto Venezolano de Investigaciones Cientificas) syndrome722019000
- IVIC syndrome722019000
- Oculo-oto-radial syndrome722019000
- Oculootoradial syndrome722019000
- Erythrokeratodermia variabilis 3722035007
- Erythrokeratodermia variabilis Kamouraska type722035007
- Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome722035007
- MEDNIK (mental retardation, enteropathy, deafness, peripheral neuropathy, ichtyosis, keratodermia) syndrome722035007
- MEDNIK syndrome722035007
- Palmoplantar keratoderma with deafness syndrome722203001
- Congenital hereditary facial palsy with variable deafness722389002
- Congenital hereditary facial paralysis with variable hearing loss syndrome722389002
- PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract) syndrome723452007
- PHARC syndrome723452007
- Peripheral neuropathy Fiskerstrand type723452007
- Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome723452007
- Congenital deafness with split hands and feet723611008
- Split hand, split foot malformation with sensorineural hearing loss syndrome723611008
- Edwards Patton Dilly syndrome724093004
- Nephropathy, deafness, hyperparathyroidism syndrome724093004
- Caudal appendage deafness syndrome726621009
- Lynch Lee Murday syndrome726621009
- Central nervous system calcification, deafness, tubular acidosis, anaemia syndrome726669007
- Central nervous system calcification, deafness, tubular acidosis, anemia syndrome726669007
- Yoshimura Takeshita syndrome726669007
- Mitochondrial myopathy, lactic acidosis, deafness syndrome732951005
- Mitochondrial myopathy, lactic acidosis, hearing loss syndrome732951005
- Dysmorphism, short stature, deafness, disorder of sex development syndrome733050004
- Dysmorphism, short stature, deafness, pseudohermaphroditism syndrome733050004
- Myoclonus, cerebellar ataxia, deafness syndrome733065003
- Deafness, small bowel diverticulosis, neuropathy syndrome733071009
- Groll Hirschowitz syndrome733071009
- Fitzsimmons Walson Mellor syndrome733089005
- Spastic paraplegia, nephritis, deafness syndrome733089005
- Mild acquired hearing loss737047001
- Moderate acquired hearing loss737048006
- Severe acquired hearing loss737049003
- Profound acquired hearing loss737050003
- Congenital mixed conductive and sensorineural hearing loss737377004
- Peripheral neuropathy, myopathy, hoarseness, deafness syndrome782752005
- Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome782752005
- Hereditary hearing loss788953003
- Peripheral sensory neuropathy789588003
- Conductive hearing loss of right ear1010236009
- Conductive hearing loss of left ear1010238005
- Autosomal dominant distal hereditary motor neuropathy1156837002
- Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome1169356004
- Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, deafness syndrome1187039001
- Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome1187039001
- Hyaluronidase 2 deficiency1187039001
- Autosomal recessive spinocerebellar ataxia type 31204415006
- Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome1204415006
- Autosomal recessive spinocerebellar ataxia, blindness, hearing loss syndrome1204415006
- SCAR3 - spinocerebellar ataxia autosomal recessive type 31204415006
- Profound hearing loss1230412003
- Isolated genetic deafness1260199008
- Isolated genetic hearing loss1260199008
- Non-syndromic genetic deafness1260199008
- Non-syndromic genetic hearing loss1260199008
- Mitchell syndrome1300194008
- Bilateral congenital malformation of external ears15983231000119107
- Congenital malformation of bilateral external ears15983231000119107
- Congenital malformation of both external ears15983231000119107
- Bilateral optic atrophy of eyes15632891000119109
- Optic atrophy of bilateral eyes15632891000119109
- Optic atrophy of both eyes15632891000119109
- Medication non-adherence due to hearing impairment454191000124106
- Mild to moderate hearing loss21451000119101
- Mixed conductive and sensorineural hearing loss of left ear18701000119107
- Mixed conductive and sensorineural hearing loss of right ear18711000119105
- Perception of hearing loss14230001000004101
- Severe hearing loss3561000119106
- Usher syndrome type 1F514793471000119104
Frequently Asked Questions
What is the ICD-10 code for unspecified hearing loss, unspecified ear?
The ICD-10-CM code for unspecified hearing loss, unspecified ear is H91.90. The full clinical description is "Unspecified hearing loss, unspecified ear". H91.90 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H91.90 mean?
ICD-10-CM code H91.90 represents "Unspecified hearing loss, unspecified ear". 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 H91.90 a billable code?
Yes, H91.90 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H91.90 in?
H91.90 is in Chapter 8: Diseases of the Ear and Mastoid Process (codes H60-H95).
What codes cannot be used with H91.90?
H91.90 has Excludes1 notes indicating codes that cannot be used together with it, including: abnormal auditory perception (H93.2-); hearing loss as classified in H90.-; impacted cerumen (H61.2-); and 3 more.
What SNOMED CT codes does H91.90 map to?
H91.90 maps to 126 SNOMED CT concepts: 205358006, 718574003, 721294001, 239010003, 427772009, and 121 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H91.90?
H91.90 is linked to 1 UMLS Concept Unique Identifier: C2881961. 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.