Other disorders of tyrosine metabolism. E70.29 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM E70.29 became effective on October 1, 2018.
Tyrosinemia. A group of disorders which have in common elevations of tyrosine in the blood and urine secondary to an enzyme deficiency. Type i tyrosinemia features episodic weakness, self-mutilation, hepatic necrosis, renal tubular injury, and seizures and is caused by a deficiency of the enzyme fumarylacetoacetase.
It is characterized by deficiency of one of the enzymes that are involved in the metabolism of tyrosine. It results in elevated blood tyrosine levels and accumulation of tyrosine and its byproducts in the liver, kidney, nervous system and other organs.
It results in elevated blood tyrosine levels and accumulation of tyrosine and its byproducts in the liver, kidney, nervous system and other organs. Group of disorders which have in common elevations of tyrosine in the blood and urine secondary to an enzyme deficiency.
F01-F99 - Mental, Behavioral and Neurodevelopmental disorders. F40-F48 - Anxiety, dissociative, stress-related, somatoform and other nonpsychotic mental disorders. F48 - Other nonpsychotic mental disorders.
ICD-10 code E88. 01 for Alpha-1-antitrypsin deficiency is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .
ICD-10-CM Code for Postmenopausal bleeding N95. 0.
4: Mixed disorder of acid-base balance.
The only specific therapy for alpha-1 antitrypsin deficiency (AATD) is augmentation therapy. During this therapy, preparations of alpha-1 antitrypsin protein that have been isolated from pooled blood of healthy donors are given by weekly intravenous infusion.
What Are the Symptoms of AAT Deficiency?Shortness of breath.Excessive cough with phlegm/sputum production.Wheezing.Decrease in exercise capacity and a persistent low energy state or tiredness.Chest pain that increases when breathing in.
ICD-10 code N85 for Other noninflammatory disorders of uterus, except cervix is a medical classification as listed by WHO under the range - Diseases of the genitourinary system .
ICD-10-CM Code for Gastro-esophageal reflux disease without esophagitis K21. 9.
83 – Other Fatigue. Code R53. 83 is the diagnosis code used for Other Fatigue.
2 - Acidosis is a sample topic from the ICD-10-CM. To view other topics, please log in or purchase a subscription. ICD-10-CM 2022 Coding Guide™ from Unbound Medicine.
pH imbalance causes A blood pH imbalance can lead to two conditions: acidosis and alkalosis. Acidosis refers to having blood that's too acidic, or a blood pH of less than 7.35. Alkalosis refers to having blood that's too basic, or a blood pH of higher than 7.45.
ICD-10-CM Code for MELAS syndrome E88. 41.
Alkaptonuria (black urine disease, black bone disease, or alcaptonuria) is a rare inherited genetic disorder in which the body cannot process the amino acids phenylalanine and tyrosine, which occur in protein.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E70.20. 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 E70.20 and a single ICD9 code, 270.2 is an approximate match for comparison and conversion purposes.
Alkaptonuria (black urine disease, black bone disease, or alcaptonuria) is a rare inherited genetic disorder in which the body cannot process the amino acids phenylalanine and tyrosine, which occur in protein.
Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded together. Excludes 1 means "do not code here."
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E70.2. Click on any term below to browse the alphabetical index.
Alkaptonuria (black urine disease, black bone disease, or alcaptonuria) is a rare inherited genetic disorder in which the body cannot process the amino acids phenylalanine and tyrosine, which occur in protein.
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.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E70.29. 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 E70.29 and a single ICD9 code, 270.2 is an approximate match for comparison and conversion purposes.