icd 10 code for glutaric aciduria type 2

What is the ICD 10 code for aciduria?

Glutaric aciduria type II. E71.313 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2020 edition of ICD-10-CM E71.313 became effective on October 1, 2019. This is the American ICD-10-CM version of E71.313 - other international versions of ICD-10 E71.313 may differ.

What is the diagnosis code for glutaric acidemia type 1?

Glutaric acidemia type I is caused by mutations in the GCDH gene; it has an autosomal recessive pattern of inheritance. Names and Codes Condition:1 Glutaric acidemia type I Abbreviation:1 GA-1 Category:2 Core SNOMED CT Code:3 76175005—Glutaric aciduria, type 1

What is the ICD 10 code for Type 1 exclude?

E71.313 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 E71.313 became effective on October 1, 2018. This is the American ICD-10-CM version of E71.313 - other international versions of ICD-10 E71.313 may differ. A type 1 excludes note is a pure excludes.

What are the signs and symptoms of glutaric acidemia type I?

In most cases, signs and symptoms first occur in infancy or early childhood and include macrocephaly, spasms, jerking, rigidity, decreased muscle tone, bleeding in the brain or eyes, and intellectual disability. Glutaric acidemia type I is caused by mutations in the GCDH gene; it has an autosomal recessive pattern of inheritance.

What is glutaric acidemia?

Glutaric acidemia type I (also called glutaric aciduria type I) is an inherited disorder in which the body is unable to process certain proteins properly. It is classified as an organic acid disorder, which is a condition that leads to an abnormal buildup of particular acids known as organic acids.

What are the symptoms of glutaric acidemia?

Signs & SymptomsIrritability.Jitteriness.Nausea, vomiting, diarrhea.Hypotonia (low muscle tone)Poor appetite or difficulty feeding.Lack of energy/sleepy.Muscle weakness.

How is glutaric acidemia treated?

Glutaric aciduria type II is treated with a high carbohydrate, low protein and low fat diet. It is recommended that affected individuals eat often to avoid low blood sugar. Dietary supplementation with riboflavin, carnitine & other supplements may be helpful.

How common is glutaric acidemia 1?

Glutaric aciduria type I (synonym, glutaric acidemia type I) is an autosomal recessive disease caused by inherited deficiency of glutaryl-CoA dehydrogenase (GCDH, EC 1.3. 99.7). It has an estimated prevalence of 1 in 100,000 newborns (Lindner et al. 2004).

How is glutaric acidemia diagnosis?

This involves pricking your baby's heel to collect drops of blood to test. If GA1 is diagnosed, treatment can be given straight away to reduce the risk of serious complications. With early diagnosis and the correct treatment, the majority of children with GA1 are able to live normal, healthy lives.

Is glutaric acid a fatty acid?

Glutaric acid is an alpha,omega-dicarboxylic acid that is a linear five-carbon dicarboxylic acid. It has a role as a human metabolite and a Daphnia magna metabolite. It is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid.

What is methylmalonic acidemia?

The methylmalonic acidemias are organic acidemias caused by an enzymatic defect in the metabolism of four amino acids (methionine, threonine, isoleucine and valine). This results in an abnormally high level of acid in the blood (academia) and body tissues.

What does Mcadd mean?

MCADD is a lifelong condition that's present from birth. It's estimated to affect up to 1 in every 10,000 babies born in the UK and is usually picked up using the newborn blood spot test. MCADD stands for medium-chain acyl-CoA dehydrogenase deficiency.

What is metabolic crisis?

This is a serious health condition caused by low blood sugar and the build-up of toxic substances in the blood. Symptoms of a metabolic crisis are poor appetite, nausea, vomiting, diarrhea, extreme sleepiness, irritable mood and behavior changes.

What is Tyrosinemia disease?

Tyrosinemia is a genetic disorder characterized by disruptions in the multistep process that breaks down the amino acid tyrosine, a building block of most proteins. If untreated, tyrosine and its byproducts build up in tissues and organs, which can lead to serious health problems.

What disease is GA?

Glutaric acidemia, type I (GA-1) is an inherited condition in which the body is unable to break down certain proteins properly. It is considered an organic acid condition because GA-1 can lead to a harmful amount of organic acids and toxins in the body.

The ICD code E713 is used to code Fatty-acid metabolism disorder

A broad classification for genetic disorders that result from an inability of the body to produce or utilize one enzyme that is required to oxidize fatty acids. The enzyme can be missing or improperly constructed, resulting in it not working. This leaves the body unable to produce energy within the liver and muscles from fatty acid sources.

Coding Notes for E71.313 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.

ICD-10-CM Alphabetical Index References for 'E71.313 - Glutaric aciduria type II'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E71.313. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

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 E71.313 and a single ICD9 code, 277.85 is an approximate match for comparison and conversion purposes.