22 result found:

Transient ischemic deafness, bilateral
Bilateral transient ischemic deafness; Transient ischemic deafness of bilateral ears
ICD-10-CM Diagnosis Code H93.013

Transient ischemic deafness, bilateral

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Transient ischemic deafness, right ear
Right ear transient ischemic deafness; Transient ischemic deafness of right ear
ICD-10-CM Diagnosis Code H93.011

Transient ischemic deafness, right ear

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Transient ischemic deafness, left ear
Left ear transient ischemic deafness; Transient ischemic deafness of left ear
ICD-10-CM Diagnosis Code H93.012

Transient ischemic deafness, left ear

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Family history of deafness and hearing loss
Family history of deafness; Family history of hearing loss; Fh: deafness; Conditions classifiable to H90-H91
ICD-10-CM Diagnosis Code Z82.2

Family history of deafness and hearing loss

    2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
Applicable To
  • Conditions classifiable to H90-H91
Transient ischemic deafness
ICD-10-CM Diagnosis Code H93.01

Transient ischemic deafness

    2016 2017 2018 2019 2020 2021 Non-Billable/Non-Specific Code
Unspecified hearing loss
Deafness NOS; High frequency deafness; Low frequency deafness
ICD-10-CM Diagnosis Code H91.9

Unspecified hearing loss

    2016 2017 2018 2019 2020 2021 Non-Billable/Non-Specific Code
Applicable To
  • Deafness NOS
  • High frequency deafness
  • Low frequency deafness
Transient ischemic deafness, unspecified ear
ICD-10-CM Diagnosis Code H93.019

Transient ischemic deafness, unspecified ear

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Ototoxic hearing loss, unspecified ear
Ototoxic hearing loss; Toxic deafness
ICD-10-CM Diagnosis Code H91.09

Ototoxic hearing loss, unspecified ear

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Congenital malformations of ear causing impairment of hearing
Congenital malform of ear causing impairment of hearing; congenital deafness (H90.-)
ICD-10-CM Diagnosis Code Q16
  • Q16 Congenital malformations of ear causing impai...
    • Q16.0 Congenital absence of (ear) auricle
    • Q16.1 Congenital absence, atresia and stricture of ...
    • Q16.2 Absence of eustachian tube
    • Q16.3 Congenital malformation of ear ossicles
    • Q16.4 Other congenital malformations of middle ear
    • Q16.5 Congenital malformation of inner ear
    • Q16.9 Congenital malformation of ear causing impair...
Unspecified hearing loss, unspecified ear
Complete deafness; Congenital hearing disorder; Deafness; Hearing disorder, congenital; Hearing loss; Hearing loss, high frequency; Hearing loss, severe; Hearing problem; Severe hearing loss; Speech and language developmental delay due to hearing loss; Speech, language developmental delay from hearing loss; Upper frequency deafness
ICD-10-CM Diagnosis Code H91.90

Unspecified hearing loss, unspecified ear

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Other and unspecified hearing loss
abnormal auditory perception (H93.2-); hearing loss as classified in H90.-; impacted cerumen (H61.2-); noise-induced hearing loss (H83.3-); psychogenic deafness (F44.6); transient ischemic deafness (H93.01-)
ICD-10-CM Diagnosis Code H91
  • H91 Other and unspecified hearing loss
Unspecified sensorineural hearing loss
Autoimmune sensorineural hearing loss; Congenital deafness; Deafness, congenital; Hearing loss sensory, unilateral; Hearing loss, sensorineural; Hearing loss, sensorineural, autoimmune; Hearing loss, sensorineural, high frequency; High frequency deafness; Keratitis ichthyosis and deafness syndrome; Kid syndrome; Kid syndrome (eye condition); Left sensory hearing loss; Neural hearing loss; Right sensory hearing loss; Sensorineural hearing loss; Unilateral sensory hearing loss; abnormal auditory perception (H93.2-); psychogenic deafness (F44.6); Central hearing loss NOS; Congenital deafness NOS; Neural hearing loss NOS; Perceptive hearing loss NOS; Sensorineural deafness NOS; Sensory hearing loss NOS
ICD-10-CM Diagnosis Code H90.5

Unspecified sensorineural hearing loss

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To
  • Central hearing loss NOS
  • Congenital deafness NOS
  • Neural hearing loss NOS
  • Perceptive hearing loss NOS
  • Sensorineural deafness NOS
  • Sensory hearing loss NOS
Type 1 Excludes
  • abnormal auditory perception (H93.2-)
  • psychogenic deafness (F44.6)
Congenital ichthyosis, unspecified
Congenital ichthyosis of skin; Ichthyosis of skin, congenital; Keratitis ichthyosis and deafness syndrome; Kid syndrome; Kid syndrome (eye condition); Netherton syndrome; Netherton's syndrome
ICD-10-CM Diagnosis Code Q80.9

Congenital ichthyosis, unspecified

    2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
Conductive and sensorineural hearing loss
deaf nonspeaking NEC (H91.3); deafness NOS (H91.9-); hearing loss NOS (H91.9-); noise-induced hearing loss (H83.3-); ototoxic hearing loss (H91.0-); sudden (idiopathic) hearing loss (H91.2-)
ICD-10-CM Diagnosis Code H90
  • H90 Conductive and sensorineural hearing loss
    • H90.0 Conductive hearing loss, bilateral
    • H90.1 Conductive hearing loss, unilateral with unre...
      • H90.11 Conductive hearing loss, unilateral, right ea...
      • H90.12 Conductive hearing loss, unilateral, left ear...
    • H90.2 Conductive hearing loss, unspecified
    • H90.3 Sensorineural hearing loss, bilateral
    • H90.4 Sensorineural hearing loss, unilateral with u...
      • H90.41 Sensorineural hearing loss, unilateral, right...
      • H90.42 Sensorineural hearing loss, unilateral, left ...
    • H90.5 Unspecified sensorineural hearing loss
    • H90.6 Mixed conductive and sensorineural hearing lo...
    • H90.7 Mixed conductive and sensorineural hearing lo...
      • H90.71 Mixed conductive and sensorineural hearing lo...
      • H90.72 Mixed conductive and sensorineural hearing lo...
    • H90.8 Mixed conductive and sensorineural hearing lo...
    • H90.A Conductive and sensorineural hearing loss wit...
      • H90.A1 Conductive hearing loss, unilateral, with res...
        • H90.A11 Conductive hearing loss, unilateral, right ea...
        • H90.A12 Conductive hearing loss, unilateral, left ear...
      • H90.A2 Sensorineural hearing loss, unilateral, with ...
        • H90.A21 Sensorineural hearing loss, unilateral, right...
        • H90.A22 Sensorineural hearing loss, unilateral, left ...
      • H90.A3 Mixed conductive and sensorineural hearing lo...
        • H90.A31 Mixed conductive and sensorineural hearing lo...
        • H90.A32 Mixed conductive and sensorineural hearing lo...
Family history of ear disorders
Family history of ear disease; Family history of of ear disease; Fh: ear disorder; family history of deafness and hearing loss (Z82.2); Conditions classifiable to H60-H83, H92-H95
ICD-10-CM Diagnosis Code Z83.52

Family history of ear disorders

    2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
Applicable To
Type 2 Excludes
  • family history of deafness and hearing loss (Z82.2)
Conductive hearing loss, unspecified
Conductive hearing loss; Conductive hearing loss, middle ear; Left middle ear conductive hearing loss; Middle ear conductive hearing loss; Right conductive hearing loss due to disorder of middle ear; Right middle ear conductive hearing loss; Conductive deafness NOS
ICD-10-CM Diagnosis Code H90.2

Conductive hearing loss, unspecified

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To
  • Conductive deafness NOS
Central auditory processing disorder
Acquired auditory processing disorder; Auditory processing disorder; Bilateral acquired auditory processing disorder; Both sides acquired auditory processing disorder; Left acquired auditory processing disorder; Right acquired auditory processing disorder; mixed receptive-expressive language disorder (F80.2); Congenital auditory imperception; Word deafness
ICD-10-CM Diagnosis Code H93.25

Central auditory processing disorder

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To
  • Congenital auditory imperception
  • Word deafness
Type 1 Excludes
  • mixed receptive-expressive language disorder (F80.2)
Unspecified keratitis
Bilateral contact lens keratitis, unresolved; Contact lens keratitis, unresolved; Keratitis; Keratitis (eye condition); Keratitis ichthyosis and deafness syndrome; Kid syndrome; Kid syndrome (eye condition); Left contact lens keratitis, unresolved; Right contact lens keratitis, unresolved; Unresolved contact lens keratitis; Unresolved keratitis of bilateral eyes caused by contact lens; Unresolved keratitis of left eye caused by contact lens; Unresolved keratitis of right eye caused by contact lens
ICD-10-CM Diagnosis Code H16.9

Unspecified keratitis

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Conversion disorder with sensory symptom or deficit
Conversion disorder w anesthesia or sensory loss; Conversion disorder w special sensory symptom; Hysterical blindness; Psychogenic symptom of special sense organ co-occurrent and due to conversion disorder; Sensory anesthesia co-occurrent and due to conversion disorder; Conversion disorder with anesthesia or sensory loss; Conversion disorder with special sensory symptoms; Dissociative anesthesia and sensory loss; Psychogenic deafness
ICD-10-CM Diagnosis Code F44.6

Conversion disorder with sensory symptom or deficit

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To
  • Conversion disorder with anesthesia or sensory loss
  • Conversion disorder with special sensory symptoms
  • Dissociative anesthesia and sensory loss
  • Psychogenic deafness
Mixed receptive-expressive language disorder
Developmental receptive language disorder; Expressive/receptive language disorder; Language disorder, receptive; Mild receptive language delay; Mixed receptive expressive language disorder; Moderate receptive language delay; Receptive developmental language delay; Receptive language delay; Receptive language delay, mild; Receptive language delay, moderate; Receptive language delay, severe; Receptive language disorder; Severe receptive language delay; central auditory processing disorder (H93.25); dysphasia or aphasia NOS (R47.-); expressive language disorder (F80.1); expressive type dysphasia or aphasia (F80.1); word deafness (H93.25); acquired aphasia with epilepsy [Landau-Kleffner] (G40.80-); pervasive developmental disorders (F84.-); selective mutism (F94.0); intellectual disabilities (F70-F79); Developmental dysphasia or aphasia, receptive type; Developmental Wernicke's aphasia
ICD-10-CM Diagnosis Code F80.2

Mixed receptive-expressive language disorder

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To
  • Developmental dysphasia or aphasia, receptive type
  • Developmental Wernicke's aphasia
Type 1 Excludes
  • central auditory processing disorder (H93.25)
  • dysphasia or aphasia NOS (R47.-)
  • expressive language disorder (F80.1)
  • expressive type dysphasia or aphasia (F80.1)
  • word deafness (H93.25)
Type 2 Excludes
  • acquired aphasia with epilepsy [Landau-Kleffner] (G40.80-)
  • pervasive developmental disorders (F84.-)
  • selective mutism (F94.0)
  • intellectual disabilities (F70-F79)
Genetic carrier of other disease
; Carrier of charcot-marie-tooth disease; Carrier of chromosome disorder; Carrier of chromosome translocation; Carrier of classical phenylketonuria; Carrier of deafness; Carrier of duchenne muscular dystrophy; Carrier of familial adenomatous polyposis; Carrier of familial dysautonomia; Carrier of fragile x chromosome; Carrier of galactosemia; Carrier of glycogen storage disease; Carrier of hemochromatosis; Carrier of hemoglobinopathy c disorder; Carrier of hemoglobinopathy disorder; Carrier of hemoglobinopathy e disorder; Carrier of heritable cancer; Carrier of heritable disorder; Carrier of high risk cancer mutation gene; Carrier of metabolic disorder; Carrier of mitochondrial defect; Carrier of muscular dystrophy; Carrier of myotonic dystrophy; Carrier of neurogenetic disorder; Carrier of tay... of chromosomes) carrier; Deafness carrier; Duchenne muscular dystrophy carrier; Familial adenomatous
ICD-10-CM Diagnosis Code Z14.8

Genetic carrier of other disease

    2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
Maternal care for other (suspected) fetal abnormality and damage, not applicable or unspecified
affected; Clubfoot, fetus affected, antepartum; Connective tissue disorder, fetus affected; Defect, abdominal wall, fetus affected, antepartum; Disorder of fetal abdominal region; Disorder of urea cycle metabolism in fetus; Fetal abdominal wall defect; Fetal ambiguous genitalia; Fetal cardiac abnormality; Fetal cardiovascular disorder; Fetal charcot-marie-tooth disease; Fetal cleft lip; Fetal cleft palate; Fetal complex heart defect; Fetal connective tissue disorder; Fetal craniosynostosis; Fetal cystic hygroma; Fetal deafness; Fetal ear anomaly; Fetal exposure to teratogen; Fetal facial abnormality; Fetal familial hypercholesterolemia; Fetal finnish nephrosis; Fetal galactosemia; Fetal gastrointestinal abnormality; Fetal gastroschisis; Fetal genitourinary abnormality; Fetal glycogen storage disease; Fetal heart disorder; Fetal hemochromatosis; Fetal hydronephrosis; Fetal limb abnormality
ICD-10-CM Diagnosis Code O35.8XX0

Maternal care for other (suspected) fetal abnormality and damage, not applicable or unspecified

    2016 2017 2018 2019 2020 2021 Billable/Specific Code Maternity Dx (12-55 years)