icd 10 code for leukodystrophy

by Arthur Medhurst 10 min read

E75. 25 - Metachromatic leukodystrophy | ICD-10-CM.

What is diagnosis code Z71 89?

Other specified counselingICD-10 code Z71. 89 for Other specified counseling is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .

What is R53 81 diagnosis?

Other malaise2022 ICD-10-CM Diagnosis Code R53. 81: Other malaise.

What is diagnosis code R53 83?

ICD-10 | Other fatigue (R53. 83)

What is the ICD-10 Code Z13 1?

You would assign ICD-10 code Z13. 1, Encounter for screening for diabetes mellitus. This code can be found under “Screening” in the Alphabetical Index of the ICD-10 book.

What is the diagnosis for ICD-10 code R50 9?

ICD-10 code: R50. 9 Fever, unspecified | gesund.bund.de.

What is the ICD-10 code for hypothyroidism?

ICD-Code E03. 9 is a billable ICD-10 code used for healthcare diagnosis reimbursement of Hypothyroidism, Unspecified. Its corresponding ICD-9 code is 244.9.

What is the ICD-10 code for postmenopausal?

N95.1ICD-10 code N95. 1 for Menopausal and female climacteric states is a medical classification as listed by WHO under the range - Diseases of the genitourinary system .

What is CPT code for fatigue?

Code R53. 83 is the diagnosis code used for Other Fatigue. It is a condition marked by drowsiness and an unusual lack of energy and mental alertness.

Is G47 00 a billable code?

ICD-Code G47. 00 is a billable ICD-10 code used for healthcare diagnosis reimbursement of Insomnia, Unspecified. Its corresponding ICD-9 code is 780.52.

What is diagnosis code Z11 3?

For claims for screening for syphilis in pregnant women at increased risk for STIs use the following ICD-10-CM diagnosis codes: • Z11. 3 - Encounter for screening for infections with a predominantly sexual mode of transmission; • and any of: Z72.Oct 18, 2019

What is diagnosis code Z13 220?

Encounter for screening for lipoid disorders2022 ICD-10-CM Diagnosis Code Z13. 220: Encounter for screening for lipoid disorders.

What is Z00 01?

Encounter for general adult medical examination with abnormal findings. Z00. 01 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is the approximate match between ICd9 and ICd10?

This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code E75.25 and a single ICD9 code, 330.0 is an approximate match for comparison and conversion purposes.

What is the name of the disease that causes a wide range of systemic symptoms?

Fabry disease can cause a wide range of systemic symptoms. It is a form of sphingolipidosis, as it involves dysfunctional metabolism of sphingolipids. The disease is named after one of its discoverers, Johannes Fabry (June 1, 1860 – June 29, 1930). Specialty:

What is Fabry disease?

Fabry disease (/ˈfɑːbri/) (also known as Fabry's disease, Anderson-Fabry disease, angiokeratoma corporis diffusum, and alpha-galactosidase A deficiency) is a rare genetic lysosomal storage disease, inherited in an X-linked manner. Fabry disease can cause a wide range of systemic symptoms. It is a form of sphingolipidosis, ...

What is a leukodystrophy?

LEUKODYSTROPHY METACHROMATIC-. an autosomal recessive metabolic disease caused by a deficiency of cerebroside sulfatase leading to intralysosomal accumulation of cerebroside sulfate sulfoglycosphingolipids in the nervous system and other organs. pathological features include diffuse demyelination and metachromatically staining granules in many cell types such as the glial cells. there are several allelic and nonallelic forms with a variety of neurological symptoms.

What is the term for the disease that affects the brain?

The leukodystrophies are rare diseases that affect the cells of the brain. Specifically, the diseases affect the myelin sheath, the material that surrounds and protects nerve cells. Damage to this sheath slows down or blocks messages between the brain and the rest of the body. This leads to problems with

When do babies die from krabbe disease?

Most infants die during the second year of life. Late-onset krabbe disease (lokd) has first symptoms at ages 5 to 10 years, consisting of focal neurological signs, hemiparesis, cerebellar ataxia, cortical blindness, and spastic paraplegia, followed by mental and physical deterioration. Some patients survive into adulthood.

When does krabbe disease start?

Two types based on the age of onset are recognized: infantile-onset krabbe disease is marked by the appearance of symptoms at ages 3-6 months, which include irritability, frequent crying, and increase of muscle tonus.

What is hemolytic anemia?

hemolytic anemias attributable to enzyme disorders ( D55.-) A degenerative disease of the central and peripheral nervous system caused by abnormal breakdown and turnover of myelin and marked by reduced galacosylceramide beta-galactosidase activity (ec 3.2.1.46).

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