icd 10 code for oculomotor apraxia

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What is the ICD 10 code for apraxia?

Apraxia. R48.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/2019 edition of ICD-10-CM R48.2 became effective on October 1, 2018. This is the American ICD-10-CM version of R48.2 - other international versions of ICD-10 R48.2 may differ.

What is the ICD 10 code for ataxia?

Diagnosis Index entries containing back-references to G11.8: Ataxia, ataxy, ataxic R27.0 ICD-10-CM Diagnosis Code R27.0. Ataxia, unspecified 2016 2017 2018 2019 2020 Billable/Specific Code Disease, diseased - see also Syndrome spinocerebellar (hereditary) G11.9 ICD-10-CM Diagnosis Code G11.9.

What is the ICD 10 code for binocular movement?

2018/2019 ICD-10-CM Diagnosis Code H51.8. Other specified disorders of binocular movement. H51.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is the ICD 10 code for Neurologic diagnosis?

G11.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/2019 edition of ICD-10-CM G11.8 became effective on October 1, 2018. This is the American ICD-10-CM version of G11.8 - other international versions of ICD-10 G11.8 may differ.

What is the ICD-10 code for apraxia?

The diagnosis code for apraxia is R48. 2. Generally, codes in the R00-R99 series are used for organic disorders. SLPs are able to diagnose apraxia, and, as such, R48.

What K31 89?

ICD-10 code K31. 89 for Other diseases of stomach and duodenum is a medical classification as listed by WHO under the range - Diseases of the digestive system .

What is R13 11?

Dysphagia, oral phase (R13.11)

What is the ICD-10 code for speech delay?

4 for Speech and language development delay due to hearing loss is a medical classification as listed by WHO under the range - Mental, Behavioral and Neurodevelopmental disorders .

What is the ICD 10 code for dysphagia?

Code R13. 10 is the diagnosis code used for Dysphagia, Unspecified. It is a disorder characterized by difficulty in swallowing. It may be observed in patients with stroke, motor neuron disorders, cancer of the throat or mouth, head and neck injuries, Parkinson's disease, and multiple sclerosis.

What is focal foveolar hyperplasia?

Foveolar hyperplasia is a rare disorder characterized by an overgrowth of mucous cells in the stomach. In children, it may present as a localized lesion that affects the antrum primarily, called focal foveolar hyperplasia (FFH), or as a diffuse lesion, known as Ménétrier disease.

What is the ICD-10 code for Ankyloglossia?

If reporting ankyloglossia with International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM), use code Q38. 1, ankyloglossia. This code is found in Chapter 17, “Congenital Malformations, Deformations, and Chromosomal Abnormalities,” of the ICD-10-CM tabular list.

What is the ICD-10 code for CVA?

I63. 9 - Cerebral infarction, unspecified | ICD-10-CM.

Is CPT 92526 a timed code?

In accordance with coding guidance from the American Speech-Language-Hearing Association (ASHA), CPT codes 92507 (Treatment of speech, language, voice, communication, and/or auditory processing disorder; individual) and 92526 (Treatment of swallowing dysfunction and/or oral function for feeding) have no time ...

What is ICD-10 code for speech therapy?

2. F80. 2 — Mixed receptive-expressive language disorder.

What is R46 89?

R46. 89 - Other symptoms and signs involving appearance and behavior | ICD-10-CM.

Is a speech impairment a developmental disability?

Specific language impairment is one of the most common developmental disorders, affecting approximately 7 to 8 percent of children in kindergarten.

What is the ICD code for binocular movement?

ICD Code H51 is a non-billable code. To code a diagnosis of this type, you must use one of the five child codes of H51 that describes the diagnosis 'other disorders of binocular movement' in more detail. H51 Other disorders of binocular movement. NON-BILLABLE.

What is the ICD code for acute care?

Use a child code to capture more detail. ICD Code H51 is a non-billable code. To code a diagnosis of this type, you must use one of the five child codes of H51 that describes the diagnosis 'other disorders ...

What is the treatment for AOA1?

Management and treatment. No specific treatment exists for AOA1 and management is mainly supportive. It includes physical therapy for cerebellar ataxia and disabilities resulting from peripheral neuropathy; educational support for reading and writing difficulties, speech therapy for dysarthria and cognitive impairment.

What is the first manifestation of AOA1?

Cerebellar ataxia is the first manifestation of AOA1 with a mean age of onset of 4.3 years (2-10 years) and is characterized by progressive gait imbalance followed by dysarthria, and limb dysmetria. Later, peripheral axonal motor neuropathy dominates the clinical picture. Oculomotor apraxia (OMA; inability to coordinate eyes ± head movements: when the head turns toward a lateral target; the head reaches the target before the eyes) is present in almost all individuals with AOA1. Chorea is present at onset in 80% of patients and upper limb dystonia (see this term) occurs in about 50% of individuals. Additional features include square wave jerks, saccadic pursuit and gaze-evoked nystagmus, areflexia followed by severe peripheral neuropathy. Variable intellectual disability is observed.

How long does it take to become wheelchair bound after AOA1?

Prognosis. AOA1 is a progressive neurodegenerative disorder and most patients usually become wheelchair bound from seven to ten years after onset of the disease. Visit the Orphanet disease page for more resources. Last updated: 1/1/2015.

Is AOA1 autosomal recessive?

Transmission of AOA1 is autosomal recessive. Genetic counseling is recommended as each sib of an affected individual has 25% chance of being affected, 50% chance of being an asymptomatic carrier, and 25% chance of being neither affected nor a carrier.