Valid for Submission
E76.29 is a billable diagnosis code used to specify a medical diagnosis of other mucopolysaccharidoses. The code E76.29 is valid during the fiscal year 2022 from October 01, 2021 through September 30, 2022 for the submission of HIPAA-covered transactions.
The ICD-10-CM code E76.29 might also be used to specify conditions or terms like deficiency of cerebroside-sulfatase, deficiency of n-acetylgalactosamine-4-sulfatase, maroteaux-lamy syndrome, maroteaux-lamy syndrome, intermediate form, maroteaux-lamy syndrome, mild form , maroteaux-lamy syndrome, severe form, etc.
Tabular List of Diseases and Injuries
The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code E76.29:
Inclusion TermsInclusion Terms
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- beta-Glucuronidase deficiency
- Maroteaux-Lamy (mild) (severe) syndrome
- Mucopolysaccharidosis, types VI, VII
Index to Diseases and Injuries
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code E76.29 are found in the index:
- - Chondro-osteodystrophy - E76.29
- - Eccentro-osteochondrodysplasia - E76.29
- - Maroteaux-Lamy syndrome (mild) (severe) - E76.29
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Deficiency of cerebroside-sulfatase
- Deficiency of N-acetylgalactosamine-4-sulfatase
- Maroteaux-Lamy syndrome
- Maroteaux-Lamy syndrome, intermediate form
- Maroteaux-Lamy syndrome, mild form
- Maroteaux-Lamy syndrome, severe form
- Mucopolysaccharidosis, MPS-VII
- MUCOPOLYSACCHARIDOSES-. group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans mucopolysaccharides. the diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
Convert E76.29 to ICD-9 Code
The General Equivalency Mapping (GEM) crosswalk indicates an approximate mapping between the ICD-10 code E76.29 its ICD-9 equivalent. The approximate mapping means there is not an exact match between the ICD-10 code and the ICD-9 code and the mapped code is not a precise representation of the original code.
Information for Patients
Carbohydrate Metabolism Disorders
Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system (enzymes) break the food parts down into sugars and acids, your body's fuel. Your body can use this fuel right away, or it can store the energy in your body tissues. If you have a metabolic disorder, something goes wrong with this process.
Carbohydrate metabolism disorders are a group of metabolic disorders. Normally your enzymes break carbohydrates down into glucose (a type of sugar). If you have one of these disorders, you may not have enough enzymes to break down the carbohydrates. Or the enzymes may not work properly. This causes a harmful amount of sugar to build up in your body. That can lead to health problems, some of which can be serious. Some of the disorders are fatal.
These disorders are inherited. Newborn babies get screened for many of them, using blood tests. If there is a family history of one of these disorders, parents can get genetic testing to see whether they carry the gene. Other genetic tests can tell whether the fetus has the disorder or carries the gene for the disorder.
Treatments may include special diets, supplements, and medicines. Some babies may also need additional treatments, if there are complications. For some disorders, there is no cure, but treatments may help with symptoms.
[Learn More in MedlinePlus]