E86.0 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 E86.0 became effective on October 1, 2019. This is the American ICD-10-CM version of E86.0 - other international versions of ICD-10 E86.0 may differ.
2016 2017 2018 2019 2020 2021 Billable/Specific Code K76.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2021 edition of ICD-10-CM K76.0 became effective on October 1, 2020. This is the American ICD-10-CM version of K76.0 - other international versions of ICD-10 K76.0 may differ.
E78.0 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail. The 2022 edition of ICD-10-CM E78.0 became effective on October 1, 2021. This is the American ICD-10-CM version of E78.0 - other international versions of ICD-10 E78.0 may differ.
K76.0 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 K76.0 became effective on October 1, 2021. This is the American ICD-10-CM version of K76.0 - other international versions of ICD-10 K76.0 may differ. A type 1 excludes note is a pure excludes.
ICD-10 code Z74. 1 for Need for assistance with personal care is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .
Hurler syndrome is caused by a deficiency of a lysosomal enzyme, IUDA, which aids in the breakdown of dermatan sulfate and heparin sulfate (GAG). This finally results in the accumulation of large amounts of GAG in the body, eventually causing the cells to become severely dysfunctional leading to death.
315.9 - Unspecified delay in development. ICD-10-CM.
E63. 9 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 E63.
What are the symptoms of Hurler syndrome?clouding of the front part of the eye (corneal clouding)frequent upper respiratory infections.enlarged tonsils and/or adenoids.distinct facial features (coarse facial features)hernias.
Williams syndrome, also known as Williams-Beuren syndrome, is a rare genetic disorder characterized by growth delays before and after birth (prenatal and postnatal growth retardation), short stature, a varying degree of mental deficiency, and distinctive facial features that typically become more pronounced with age.
There are four main types of developmental disorders: nervous system disabilities, sensory related disabilities, metabolic disabilities and degenerative disorders. Many different subsets of disabilities nest under these four main groups.
Z13. 4*- Encounter for screening for certain developmental disorders in childhood.
ICD-10 code R62. 50 for Unspecified lack of expected normal physiological development in childhood is a medical classification as listed by WHO under the range - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified .
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 .
Medical nutritional therapy codes (97802, 97803, S9470) may be billed when counseling patients on obesity or weight management. These codes are compatible with any diagnosis but are most appropriate or intended for illness or disease-related diagnoses such as obesity or diabetes.
The 2022 edition of ICD-10-CM Z76. 0 became effective on October 1, 2021. This is the American ICD-10-CM version of Z76.
Symptoms most often begin to appear between ages 3 and 8. Children with Hurler syndrome may have unusually large heads, joint stiffness, hearing and vision loss, impaired growth, and other symptoms. The medical name for Hurler syndrome is mucopolysaccharidosis type I.
Mucopolysaccharidosis type 1 (MPS 1) is a rare lysosomal storage disease, which is an inherited metabolic disease. While there is no cure for Hurler syndrome, treatment does exist.
No cure is available for Hunter syndrome. The most severe cases can be life-threatening, with life expectancy typically between 10 and 20 years. People with mild cases of the disease typically live longer into adulthood.
MPS I is inherited, which means that your parents must pass the disease on to you. If both parents carry a nonworking copy of the gene related to this condition, each of their children has a 25% (1 in 4) chance of developing the disease. People with MPS I do not make an enzyme called lysosomal alpha-L-iduronidase.
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 E76.0. Click on any term below to browse the alphabetical index.
The 2022 edition of ICD-10-CM E78.0 became effective on October 1, 2021.
Clinical Information. A group of familial disorders characterized by elevated circulating cholesterol contained in either low-density lipoproteins alone or also in very-low-density lipoproteins (pre-beta lipoproteins).
code (s) for any associated disorders of electrolyte and acid-base balance ( E87.-) A condition caused by the loss of too much water from the body. Severe diarrhea or vomiting can cause dehydration. A condition resulting from the excessive loss of water from the body.
The 2022 edition of ICD-10-CM E86.0 became effective on October 1, 2021.
hemolytic anemias attributable to enzyme disorders ( D55.-) code (s) for any associated disorders of electrolyte and acid-base balance ( E87.-) A condition caused by the loss of too much water from the body. Severe diarrhea or vomiting can cause dehydration.
Lysosomal storage diseases (LSDs; /ˌlaɪsəˈsoʊməl/) are a group of approximately 50 rare inherited metabolic disorders that result from defects in lysosomal function. Lysosomes are sacs of enzymes within cells that digest large molecules and pass the fragments on to other parts of the cell for recycling.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E76. Click on any term below to browse the alphabetical index.