Condition:1 | Nonketotic hyperglycinemia (glycine encephalopathy) |
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Category:2 | Other |
SNOMED CT Code:3 | 237939006—Non-ketotic hyperglycinemia UMLS CUI:4C0751748 |
ICD-9-CM Code:5 | 270.7—Other disturbances of straight-chain amino-acid metabolism |
ICD-10-CM Code:6 | E72.51—Non-ketotic hyperglycinemia |
Diagnosis Index entries containing back-references to E72.51: Disorder (of) - see also Disease glycine metabolism E72.50 ICD-10-CM Diagnosis Code E72.50 Glucoglycinuria E72.51 Glycinemia E72.51 Hyperglycinemia E72.51 (non-ketotic) Non-ketotic hyperglycinemia E72.51
‣ More Information Nonketotic hyperglycinemia (also known as glycine encephalopathy) is a genetic disorder characterized by abnormally high levels of the amino acid glycine.
E11.00 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Type 2 diab w hyprosm w/o nonket hyprgly-hypros coma (NKHHC) The 2018/2019 edition of ICD-10-CM E11.00 became effective on October 1, 2018.
secondary diabetes mellitus NEC ( E13.-) type 1 diabetes mellitus ( E10.-) Hyperosmolarity without nonketotic hyperglycemic hyperosmolar coma due to type 2 diabetes mellitus Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
Non-ketotic hyperglycinemia (NKH) is a rare, genetic, metabolic disorder caused by a defect in the enzyme system that breaks down the amino acid glycine, resulting in an accumulation of glycine in the body's tissues and fluids. There is a classical form of NKH and a variant form of NKH.
Clinical Description. Nonketotic hyperglycinemia (NKH) is the inborn error of glycine metabolism defined by deficient activity of the glycine cleavage enzyme system (GCS), which results in accumulation of large quantities of glycine in all body tissues including the brain.
Signs of nonketotic hyperglycinemia (NKH) can begin any time from infancy to adulthood and include:Sleeping longer or more often.Weak muscle tone (also known as hypotonia)Wandering eye movements.Abnormal jerky movements.Difficulty feeding.Difficulty breathing.Developmental delay.
Being a fatal disease, NKH has devastating consequences. The majority of patients die within the first week of life and those who survive suffer from severe mental retardation [11].
Hyperprolinemia, also referred to as prolinemia or prolinuria, is a condition which occurs when the amino acid proline is not broken down properly by the enzymes proline oxidase or pyrroline-5-carboxylate dehydrogenase, causing a buildup of proline in the body.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E72.51. 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 E72.51 and a single ICD9 code, 270.7 is an approximate match for comparison and conversion purposes.