E76.01 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM E76.01 became effective on October 1, 2021. This is the American ICD-10-CM version of E76.01 - other international versions of ICD-10 E76.01 may differ.
E76.01 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM E76.01 became effective on October 1, 2021.
There are three recognized phenotypes representing a spectrum of clinical severity from severe to mild: hurler's syndrome, hurler-scheie syndrome and scheie's syndrome (formerly mucopolysaccharidosis v). Symptoms may include dwarfism, hepatosplenomegaly, gargoyle-like facies, corneal clouding, cardiac complications, and noisy breathing.
Mucopolysaccharidosis, type II. E76.1 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 E76.1 became effective on October 1, 2018. This is the American ICD-10-CM version of E76.1 - other international versions of ICD-10 E76.1 may differ.
Hurler syndrome is an inherited condition caused by a faulty gene. Children with Hurler syndrome lack an enzyme that the body needs to digest sugar. As a result, undigested sugar molecules build up in the body, causing progressive damage to the brain, heart, and other organs.
E71. 510 - Zellweger syndrome | ICD-10-CM.
ICD-10 code E73. 9 for Lactose intolerance, unspecified is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .
What causes Zellweger syndrome? ZS is the result of a mutation in any of the 12 PEX genes. Most cases of ZS are due to a mutation in the PEX1 gene. These genes control peroxisomes, which are needed for normal cell function.
Zellweger spectrum disorder is estimated to occur in 1 in 50,000 individuals.
ICD-10 code Z91. 01 for Food allergy status is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .
ICD-10 code K90. 0 for Celiac disease is a medical classification as listed by WHO under the range - Diseases of the digestive system .
ICD-10-CM Code for Gastro-esophageal reflux disease without esophagitis K21. 9.
ICD-10-CM Code for Gastro-esophageal reflux disease without esophagitis K21. 9.
G40. 89 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
ICD-10 Code for Unspecified convulsions- R56. 9- Codify by AAPC.
9 – Hypothyroidism, Unspecified. ICD-Code E03. 9 is a billable ICD-10 code used for healthcare diagnosis reimbursement of Hypothyroidism, Unspecified.
Hurler syndrome, also known as mucopolysaccharidosis type I (MPS I), Hurler's disease, also gargoylism, is a genetic disorder that results in the buildup of glycosaminoglycans (formerly known as mucopolysaccharides) due to a deficiency of alpha-L iduronidase, an enzyme responsible for the degradation of mucopolysaccharides in lysosomes.:544 Without this enzyme, a buildup of heparan sulfate and dermatan sulfate occurs in the body.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E76.02. Click on any term below to browse the alphabetical index.
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 E76.02 and a single ICD9 code, 277.5 is an approximate match for comparison and conversion purposes.
The 2022 edition of ICD-10-CM E76.0 became effective on October 1, 2021.
Hunter syndrome (mucopolysaccharidosis ii) and hurler syndrome were each originally called "gargoylism" because of the coarseness of the facial features of affected individuals. The most common type of mucopolysaccharidosis. It is inherited in an autosomal recessive pattern.