Sensorineural hearing impairment

A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve.

Also called: Hearing loss, sensorineural, Sensorineural deafness, Sensorineural hearing loss.

Not sure what sensorineural hearing impairment might be related to? See the lab tests that healthcare providers may use to investigate sensorineural hearing impairment, and the conditions they help explore.
Explore relevant lab tests
Associations

Conditions associated with sensorineural hearing impairment

The following conditions have been associated with sensorineural hearing impairment in medical literature. This is informational and not a diagnosis.

1p36 deletion syndrome

1p36 deletion syndrome is a medical condition that may be associated with various symptoms and signs....

General

3-methylglutaconic aciduria type 8

3-methylglutaconic aciduria type 8 is a medical condition that may be associated with various symptoms and sig...

General

Adult-onset autosomal dominant leukodystrophy

Adult-onset autosomal dominant leukodystrophy is a medical condition that may be associated with various sympt...

General

Alobar holoprosencephaly

Alobar holoprosencephaly is a medical condition that may be associated with various symptoms and signs....

General

Alpha-mannosidosis, infantile form

Alpha-mannosidosis, infantile form is a medical condition that may be associated with various symptoms and sig...

General

Alport syndrome

Alport syndrome is a medical condition that may be associated with various symptoms and signs....

General

Alstrom syndrome

A multisystemic disorder characterized by cone-rod dystrophy, hearing loss, obesity, insulin resistance and hy...

General

Autosomal dominant Charcot-Marie-Tooth disease type 2A2

Autosomal dominant Charcot-Marie-Tooth disease type 2A2 is a medical condition that may be associated with var...

General

Autosomal dominant optic atrophy, classic form

Autosomal dominant optic atrophy, classic form is a medical condition that may be associated with various symp...

General

Autosomal dominant spastic paraplegia type 9A

Autosomal dominant spastic paraplegia type 9A is a medical condition that may be associated with various sympt...

General

Bilateral polymicrogyria

Bilateral polymicrogyria is a medical condition that may be associated with various symptoms and signs....

General

Biotinidase deficiency

Biotinidase deficiency is a medical condition that may be associated with various symptoms and signs....

General

Brown-Vialetto-van Laere syndrome 1

Any Brown-Vialetto-van Laere syndrome in which the cause of the disease is a mutation in the SLC52A3 gene....

General

Brown-Vialetto-van Laere syndrome 2

Any Brown-Vialetto-van Laere syndrome in which the cause of the disease is a mutation in the SLC52A2 gene....

General

CINCA syndrome

CINCA syndrome is a medical condition that may be associated with various symptoms and signs....

General

CODAS syndrome

Codas syndrome is a multiple congenital anomalies syndrome characterized by Cerebral, Ocular, Dental, Auricula...

General

Carey-Fineman-Ziter syndrome 1

A rare condition characterized by the association of hypotonia, Moebius sequence (bilateral congenital facial ...

General

Charcot-Marie-Tooth disease X-linked dominant 1

Charcot-Marie-Tooth neuropathy that is inherited in an X-linked manner, and is associated with mutation(s) in ...

General

Charcot-Marie-Tooth disease axonal type 2C

Autosomal dominant Charcot-Marie-Tooth disease type 2C (CMT2C) is a form of axonal Charcot-Marie-Tooth disease...

General

Charcot-Marie-Tooth disease type 1E

Charcot-Marie-Tooth disease type 1E is a medical condition that may be associated with various symptoms and si...

General

Charcot-Marie-Tooth disease type 1E

A rare subtype of CMT1 characterized by a variable clinical presentation. Onset within the first two years of ...

General

Charcot-Marie-Tooth disease type 1F

Charcot-Marie-Tooth disease type 1F is a medical condition that may be associated with various symptoms and si...

General

Charcot-Marie-Tooth disease type 4B2

Charcot-Marie-Tooth disease type 4B2 is a medical condition that may be associated with various symptoms and s...

General

Charcot-Marie-Tooth disease type 4C

Charcot-Marie-Tooth disease type 4C is a medical condition that may be associated with various symptoms and si...

General

Cockayne syndrome type 1

Cockayne syndrome caused by mutation(s) in the ERCC8 gene, encoding DNA excision repair protein ERCC-8....

General

Cockayne syndrome type 2

Cockayne syndrome caused by mutation(s) in the ERCC6 gene, encoding DNA excision repair protein ERCC-6....

General

Coffin-Siris syndrome 12

Coffin-Siris syndrome 12 is a medical condition that may be associated with various symptoms and signs....

General

Congenital myasthenic syndrome

Congenital myasthenic syndrome is a medical condition that may be associated with various symptoms and signs....

General

Cornelia de Lange syndrome 1

Any Cornelia de Lange syndrome in which the cause of the disease is a mutation in the NIPBL gene....

General

D-glyceric aciduria

A metabolic disorder characterized by D-glyceric acid excretion. It has been described in several patients. Cl...

General

DEGCAGS syndrome

DEGCAGS syndrome is a medical condition that may be associated with various symptoms and signs....

General

Distal renal tubular acidosis

Distal renal tubular acidosis is a medical condition that may be associated with various symptoms and signs....

General

Fabry disease

Fabry disease is a medical condition that may be associated with various symptoms and signs....

General

Facioscapulohumeral dystrophy

Facioscapulohumeral dystrophy is a medical condition that may be associated with various symptoms and signs....

General

Familial cold urticaria

Familial cold urticaria is a medical condition that may be associated with various symptoms and signs....

General

Folinic acid-responsive seizures

Folinic acid-responsive seizures is a medical condition that may be associated with various symptoms and signs...

General

Full NF2-related schwannomatosis

Full NF2-related schwannomatosis is a medical condition that may be associated with various symptoms and signs...

General

GATA2 deficiency spectrum

GATA2 deficiency spectrum is a medical condition that may be associated with various symptoms and signs....

General

Generalized arterial calcification of infancy

Generalized arterial calcification of infancy is a medical condition that may be associated with various sympt...

General

Granulomatosis with polyangiitis

Granulomatosis with polyangiitis is a medical condition that may be associated with various symptoms and signs...

General

Tests

Tests providers may use to investigate sensorineural hearing impairment

When investigating sensorineural hearing impairment, a healthcare provider may order one or more of the following laboratory tests. Test selection is a clinical decision made by a qualified professional.

CBC with Differential

Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...

Sample: Blood

Comprehensive Metabolic Panel (CMP)

Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...

Sample: Blood

Electrolyte Panel

Measures sodium, potassium, chloride, and bicarbonate....

Sample: Blood

Fasting Glucose

Measures blood sugar after fasting to screen for diabetes and prediabetes....

Sample: Blood

Hemoglobin A1c (HbA1c)

Reflects average blood sugar over the past 2-3 months....

Sample: Blood

Magnesium

Measures magnesium levels, important for nerve and muscle function....

Sample: Blood

Thyroid Panel

Comprehensive thyroid testing including TSH, free T4, and free T3....

Sample: Blood

Urinalysis

Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....

Sample: Urine

Related

Symptoms commonly seen alongside sensorineural hearing impairment

When to seek care

Seek care from a qualified healthcare provider if sensorineural hearing impairment is severe, persistent, worsening, or accompanied by concerning symptoms. If you think you have a medical emergency, call your local emergency number immediately.

FAQ

Frequently Asked Questions

What does the symptom sensorineural hearing impairment mean?

Sensorineural hearing impairment is a health sign or symptom described in medical literature. A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve.

Which conditions are associated with sensorineural hearing impairment?

Sensorineural hearing impairment has been reported in association with 136 conditions in the medical literature we index, including 1p36 deletion syndrome, 3-methylglutaconic aciduria type 8, Adult-onset autosomal dominant leukodystrophy, Alobar holoprosencephaly, Alpha-mannosidosis, infantile form. These associations do not mean you have any of these conditions.

Should I see a doctor about sensorineural hearing impairment?

You should discuss any persistent or concerning symptoms with a qualified healthcare provider. This website does not provide diagnosis. If you have severe symptoms or signs of a medical emergency, seek care immediately.

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