Hydrops fetalis due to isoimmunization. P56.0 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 P56.0 became effective on October 1, 2018. This is the American ICD-10-CM version of P56.0 - other international versions of ICD-10 P56.0 may differ.
Alpha thalassemia. D56.0 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 D56.0 became effective on October 1, 2018.
Hydrops fetalis due to isoimmunization 2016 2017 2018 2019 2020 2021 Billable/Specific Code Code on Newborn Record P56.0 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 P56.0 became effective on October 1, 2020.
ICD-10 code D56. 0 for Alpha thalassemia is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .
HYDROPS FETALIS is a serious disorder, usually indicative of an ominous prognosis for the affected fetus. There are many causes, including both hereditary and acquired diseases. 1-3 In southeast Asia, α-thalassemia is the most common cause of fetal hydrops, accounting for 60% to 90% of the cases.
Alpha thalassemia occurs when some or all of the 4 genes that make hemoglobin (the alpha-globin genes) are missing or damaged. There are 4 types of alpha thalassemia: Alpha thalassemia silent carrier. One gene is missing or damaged, and the other 3 are normal. Blood tests are usually normal.
Hb Bart's hydrops fetalis, also known as alpha thalassemia major, is the most severe form of alpha thalassemia. The term hydrops fetalis describes the accumulation of large amounts of fluid (edema) in the tissues and organs of a developing fetus.
This condition has been called hydrops fetalis, and Hb Bart's hydrops or Hb Bart's disease. Prenatal diagnosis of homozygous α-thalassemia is possible via chorionic villous sampling between the 10th and 12th weeks of gestation. Signs of hydrops can also be detected on prenatal ultrasound.
Hydrops fetalis — or hydrops — is a condition in which large amounts of fluid build up in a baby's tissues and organs, causing extensive swelling (edema).
Alpha Thalassemia Major (ATM) is an inherited autosomal recessive disease, in which two non-functioning alpha globin genes are passed from each parent to the fetus, resulting in loss of function of all four alpha globin genes in the fetus.
Alpha thalassemia major (Hb Bart syndrome). This is a very serious form that develops before birth. It causes hydrops fetalis. This is a condition in which the body has too much fluid and other serious problems. Most affected babies are stillborn.
A baby with Alpha thalassemia major does not have any normal alpha globin alleles. Their bodies cannot make any normal hemoglobin. This condition is so serious that damage to their body begins before birth and survival is rare.
When thalassemia is called “alpha” or “beta,” this refers to the part of hemoglobin that isn't being made. If either the alpha or beta part is not made, there aren't enough building blocks to make normal amounts of hemoglobin. Low alpha is called alpha thalassemia. Low beta is called beta thalassemia.
The condition occurs when a disease or medical condition affects the body's ability to manage fluid. There are three main causes for this type, heart or lung problems, severe anemia (such as from thalassemia or infections), and genetic or developmental problems, including Turner syndrome.
Alpha (α) thalassemia is a hereditary disorder and is caused by deletions or mutations in globin genes. It is present in two clinically significant forms: hemoglobin Bart hydrops fetalis (Hb Bart) syndrome and hemoglobin H (HbH) disease. It is highly prevalent in South-East Asia or Mediterranean countries.
The condition occurs when a disease or medical condition affects the body's ability to manage fluid. There are three main causes for this type, heart or lung problems, severe anemia (such as from thalassemia or infections), and genetic or developmental problems, including Turner syndrome.
Beta thalassemia is a blood disorder that reduces the production of hemoglobin . Hemoglobin is the iron-containing protein in red blood cells that carries oxygen to cells throughout the body. In people with beta thalassemia, low levels of hemoglobin lead to a lack of oxygen in many parts of the body.
Beta thalassemia intermedia. People with beta thalassemia intermedia have moderately severe anemia and some will need blood transfusions and other medical treatment. Blood transfusions deliver healthy hemoglobin and RBCs to the body. Beta thalassemia major (also called Cooley's anemia).
This condition is called thalassemia minor or beta-thalassemia. Two mutated genes, your signs and symptoms will be moderate to severe. This condition is called thalassemia major, or Cooley anemia.
Hydrops fetalis is a condition in the fetus characterized by an accumulation of fluid, or edema, in at least two fetal compartments. By comparison, hydrops allantois or hydrops amnion are an accumulation of excessive fluid in the allantoic or amniotic space respectively.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code P56.99. 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 P56.99 and a single ICD9 code, 773.3 is an approximate match for comparison and conversion purposes.
Hydrops fetalis is a condition in the fetus characterized by an accumulation of fluid, or edema, in at least two fetal compartments. By comparison, hydrops allantois or hydrops amnion are an accumulation of excessive fluid in the allantoic or amniotic space respectively.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code P56.90. 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 P56.90 and a single ICD9 code, 773.3 is an approximate match for comparison and conversion purposes.
Hydrops fetalis is a condition in the fetus characterized by an accumulation of fluid, or edema, in at least two fetal compartments. By comparison, hydrops allantois or hydrops amnion are an accumulation of excessive fluid in the allantoic or amniotic space respectively.
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 P56. Click on any term below to browse the alphabetical index.