Diagnosis Code

H90.5 UNSPECIFIED SENSORINEURAL HEARING LOSS


Code Information

Diagnosis Code: H90.5

Short Description: Unspecified sensorineural hearing loss

Long Description: Unspecified sensorineural hearing loss

The code H90.5 is VALID for claim submission

Code Classification:

  • Diseases of the ear and mastoid process (H60–H95)
    • Other disorders of ear (H90-H94)
      • Conductive and sensorineural hearing loss (H90)
        • H90.5 Unspecified sensorineural hearing loss

Code Version: 2022 ICD-10-CM


Synonyms

  • 10p partial monosomy syndrome
  • 3-Methylglutaconic aciduria type 4
  • 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
  • Achalasia of esophagus
  • Acquired sensorineural hearing loss
  • Acquired sensorineural hearing loss
  • Acquired sensorineural hearing loss
  • Acquired sensorineural hearing loss
  • Acquired sensorineural hearing loss
  • Albinism with deafness syndrome
  • Anal atresia
  • Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome
  • Arts syndrome
  • Asymmetrical hearing loss
  • Asymmetrical sensorineural hearing loss
  • Auditory synaptopathy
  • Autoimmune sensorineural hearing loss
  • Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
  • Autosomal dominant deafness with onychodystrophy syndrome
  • Autosomal dominant ichthyosis
  • Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome
  • Autosomal dominant retinitis pigmentosa
  • Autosomal recessive keratitis-ichthyosis-deafness syndrome
  • Benign neoplasm of sacrococcygeal region
  • Black locks, oculocutaneous albinism, AND deafness of the sensorineural type
  • Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
  • Central hearing loss
  • Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
  • Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
  • Chitty Hall Baraitser syndrome
  • Chronic deafness
  • Chronic deafness
  • Combined perceptive hearing loss
  • Complete deafness
  • Complete deafness
  • Complete deafness
  • Complete deafness
  • Complete deafness
  • Congenital achalasia of esophagus
  • Congenital atrophy of optic nerve
  • Congenital calyceal diverticulum
  • Congenital cataract with ataxia and deafness syndrome
  • Congenital cataract with deafness and hypogonadism syndrome
  • Congenital cataract, hearing loss, severe developmental delay syndrome
  • Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
  • Congenital conductive hearing loss
  • Congenital corneal dystrophy
  • Congenital deafness
  • Congenital deafness
  • Congenital deafness
  • Congenital deafness
  • Congenital dilatation of colon
  • Congenital hearing disorder
  • Congenital hereditary endothelial dystrophy
  • Congenital hereditary endothelial dystrophy and perceptive deafness syndrome
  • Congenital kyphoscoliosis
  • Congenital kyphosis
  • Congenital nephritis
  • Congenital osteodystrophy
  • Congenital prelingual deafness
  • Congenital sensorineural hearing loss
  • Craniofacial deafness hand syndrome
  • Cutaneous syndrome with ichthyosis
  • Cutaneous syndrome with ichthyosis
  • Cutaneous syndrome with ichthyosis
  • Deafness and hypogonadism syndrome
  • Deafness and oligodontia syndrome
  • Deafness craniofacial syndrome
  • Deafness with onychodystrophy syndrome
  • Deafness with onychodystrophy syndrome
  • Deafness, encephaloneuropathy, obesity, valvulopathy syndrome
  • Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
  • Deafness, vitiligo, achalasia syndrome
  • Deafness-dystonia-optic neuronopathy syndrome
  • Deletion of part of chromosome 10
  • Deletion of part of chromosome 11
  • Dentinogenesis imperfecta
  • Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
  • Developmental malformation, deafness, dystonia syndrome
  • Diabetes-deafness syndrome maternally transmitted
  • DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome
  • Distal renal tubular acidosis
  • Distal renal tubular acidosis co-occurrent with sensorineural deafness
  • Diverticulum of renal calyx
  • Dominant sensorineural hearing loss
  • DOORS syndrome
  • Duane retraction syndrome with congenital deafness
  • Duane's syndrome, type 3
  • Ectodermal dysplasia and sensorineural deafness syndrome
  • Ehlers-Danlos syndrome kyphoscoliotic and deafness type
  • Ehlers-Danlos syndrome kyphoscoliotic type
  • End organ deafness
  • Epiphyseal dysplasia, hearing loss, dysmorphism syndrome
  • Essential tremor
  • Familial steroid-resistant nephrotic syndrome with sensorineural deafness
  • Gemignani syndrome
  • Generalized dystonia
  • Gingival fibromatosis
  • Gingival fibromatosis with progressive deafness syndrome
  • Globodontia
  • Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
  • Hereditary essential tremor
  • Hereditary gingival fibromatosis
  • Hereditary growth hormone deficiency
  • Hereditary sensory neuropathy
  • Heritable disorder of neutrophil function
  • High frequency sensorineural hearing loss in right ear
  • Hirschsprung disease with deafness and polydactyly syndrome
  • Hypertelorism
  • Hypertelorism, preauricular sinus, punctual pits, deafness syndrome
  • Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
  • Hypoparathyroidism, deafness, renal disease syndrome
  • Hypotrichosis and deafness syndrome
  • Kawashima Tsuji syndrome
  • Keipert syndrome
  • KID syndrome
  • KID syndrome
  • Lipoma of lower back
  • Lowe Kohn Cohen syndrome
  • Lowry Yong syndrome
  • Macrodontia
  • Male infertility of chromosomal origin
  • Mandibular hypoplasia, deafness, progeroid syndrome
  • Maternal perinatal sensorineural hearing loss
  • Maternally inherited cardiomyopathy and hearing loss syndrome
  • Megaloblastic anemia due to inborn errors of metabolism
  • Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
  • Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome
  • Micromelia
  • Multiple malformation syndrome, moderate short stature, facial
  • Narcolepsy
  • Nathalie syndrome
  • Neonatal sensorineural hearing loss
  • Nephrosis, deafness, urinary tract, digital malformation syndrome
  • Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome
  • Neural hearing loss
  • Neural hearing loss
  • Neural hearing loss of left ear
  • Neural hearing loss of right ear
  • Neutropenia, monocytopenia, deafness syndrome
  • Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome
  • Non-syndromic mitochondrial sensorineural deafness
  • Ocular albinism
  • Ocular albinism with late-onset sensorineural deafness
  • Oculootodental syndrome
  • Oligodontia
  • Olivopontocerebellar atrophy and deafness
  • Olivopontocerebellar degeneration
  • Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome
  • Panhypopituitarism
  • PCNA-related progressive neurodegenerative photosensitivity syndrome
  • Peripheral neuropathy with sensorineural hearing impairment syndrome
  • Phocomelia
  • Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome
  • Pili torti
  • Pili torti-deafness syndrome
  • Postnatal acquired sensorineural hearing loss
  • Postoperative profound sensorineural hearing loss
  • Preauricular fistula
  • Premature canities
  • Primary hypersomnia
  • Profound acquired hearing loss
  • Profound hearing loss
  • Profound hearing loss
  • Profound sensorineural hearing loss
  • Profound sensorineural hearing loss
  • Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome
  • Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome
  • Recessive sensorineural hearing loss
  • Recessive sensorineural hearing loss
  • Renal caliceal diverticuli and deafness syndrome
  • Renal tubular acidosis with progressive nerve deafness
  • Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome
  • Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome
  • Retinitis pigmentosa-deafness syndrome
  • Retinitis pigmentosa-deafness syndrome type 3
  • Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome
  • Sellars Beighton syndrome
  • Sensorineural deafness and male infertility
  • Sensorineural deafness due to late congenital syphilis
  • Sensorineural deafness with dilated cardiomyopathy syndrome
  • Sensorineural hearing loss
  • Sensorineural hearing loss in left ear
  • Sensorineural hearing loss in right ear
  • Sensorineural hearing loss in right ear
  • Sensorineural hearing loss of combined sites
  • Sensorineural hearing loss of left ear
  • Sensorineural hearing loss of right ear
  • Sensorineural hearing loss, early graying, essential tremor syndrome
  • Sensory hearing loss
  • Sensory hearing loss
  • Sensory neuropathy
  • Senter syndrome
  • Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome
  • Severe X-linked intellectual disability Gustavson type
  • Sinoatrial node dysfunction and deafness
  • Spondyloepiphyseal dysplasia MacDermot type
  • Steroid-resistant nephrotic syndrome
  • Sudden hearing loss
  • Sudden sensorineural hearing loss
  • Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
  • Thiamine-responsive megaloblastic anemia
  • Thong Douglas Ferrante syndrome
  • Tungland Bellman syndrome
  • Woodhouse Sakati syndrome
  • X-linked sensorineural hearing loss
  • X-linked sensorineural hearing loss

Diagnostic Related Group(s)

The code H90.5 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Other Ear, Nose, Mouth And Throat Diagnoses With Mcc (154)
  • Other Ear, Nose, Mouth And Throat Diagnoses With Cc (155)
  • Other Ear, Nose, Mouth And Throat Diagnoses Without Cc/mcc (156)

References to Index of Diseases and Injuries

The code H90.5 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • 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 Notes:
    • abnormal auditory perception (@H93.2*-)
    • psychogenic deafness (@F44.6*)

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
H90.5 Right Arrow 389.10 Sensorneur hear loss NOS
389.14 Central hearing loss
389.16 Sensoneur hear loss asym

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
H90 Conductive and sensorineural hearing loss
H90.0 Conductive hearing loss, bilateral
H90.1 Conductive hearing loss, unilateral with unrestricted hearing on the contralateral side
H90.11 Conductive hearing loss, unilateral, right ear, with unrestricted hearing on the contralateral side
H90.12 Conductive hearing loss, unilateral, left ear, with unrestricted hearing on the contralateral side
H90.2 Conductive hearing loss, unspecified
H90.3 Sensorineural hearing loss, bilateral
H90.4 Sensorineural hearing loss, unilateral with unrestricted hearing on the contralateral side
H90.41 Sensorineural hearing loss, unilateral, right ear, with unrestricted hearing on the contralateral side
H90.42 Sensorineural hearing loss, unilateral, left ear, with unrestricted hearing on the contralateral side
H90.6 Mixed conductive and sensorineural hearing loss, bilateral
H90.7 Mixed conductive and sensorineural hearing loss, unilateral with unrestricted hearing on the contralateral side
H90.71 Mixed conductive and sensorineural hearing loss, unilateral, right ear, with unrestricted hearing on the contralateral side
H90.72 Mixed conductive and sensorineural hearing loss, unilateral, left ear, with unrestricted hearing on the contralateral side
H90.8 Mixed conductive and sensorineural hearing loss, unspecified
H90.A Conductive and sensorineural hearing loss with restricted hearing on the contralateral side
H90.A1 Conductive hearing loss, unilateral, with restricted hearing on the contralateral side
H90.A11 Conductive hearing loss, unilateral, right ear with restricted hearing on the contralateral side
H90.A12 Conductive hearing loss, unilateral, left ear with restricted hearing on the contralateral side
H90.A2 Sensorineural hearing loss, unilateral, with restricted hearing on the contralateral side
H90.A21 Sensorineural hearing loss, unilateral, right ear, with restricted hearing on the contralateral side
H90.A22 Sensorineural hearing loss, unilateral, left ear, with restricted hearing on the contralateral side
H90.A3 Mixed conductive and sensorineural hearing loss, unilateral with restricted hearing on the contralateral side
H90.A31 Mixed conductive and sensorineural hearing loss, unilateral, right ear with restricted hearing on the contralateral side
H90.A32 Mixed conductive and sensorineural hearing loss, unilateral, left ear with restricted hearing on the contralateral side


This page was last updated on: 10/1/2023