D58.1 is a valid billable ICD-10 diagnosis code for Hereditary elliptocytosis . It is found in the 2022 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2021 - Sep 30, 2022 .
Hereditary spherocytosis. D58.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
D58.1 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 D58.1 became effective on October 1, 2021. This is the American ICD-10-CM version of D58.1 - other international versions of ICD-10 D58.1 may differ. hemolytic anemia of the newborn ( P55.-)
D58.1 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 D58.1 became effective on October 1, 2018. This is the American ICD-10-CM version of D58.1 - other international versions of ICD-10 D58.1 may differ.
Hereditary elliptocytosis (HE), also called hereditary ovalocytosis, is a heterogeneous group of inherited red blood cell (RBC) disorders characterized by the presence of elongated, oval, or elliptically shaped RBCs on the peripheral blood smear.
Initial laboratory studies for the diagnosis of hereditary elliptocytosis (HE) include the following :Complete blood cell count (CBC)Peripheral blood smear.Direct antiglobulin test (Coombs test)Bilirubin.Haptoglobin.Reticulocyte count/immature reticulocyte fraction.Potassium.Lactate dehydrogenase (LDH)
Code Z13. 89, encounter for screening for other disorder, is the ICD-10 code for depression screening.
Hereditary elliptocytosis is caused by a genetic change in either the EPB41, SPTA1, or SPTB gene, and is inherited in an autosomal dominant pattern.
Hereditary elliptocytosis (ovalocytosis) is a rare autosomal dominant disorder in which RBCs are oval or elliptical. Hemolysis is usually absent or slight, with little or no anemia except in some homozygous patients (hereditary pyropoikilocytosis).
Hereditary Elliptocytosis/Ovalocytosis/Pyropoikilocytosis HE and hereditary pyropoikilocytosis (HPP) are caused by mutations, which lead to failure of spectrin heterodimers to self associate into heterotetramers, the basic building blocks of the RBC membrane skeleton network.
ICD-10 code Z13. 40 for Encounter for screening for unspecified developmental delays is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .
Z03. 89 No diagnosis This diagnosis description is CHANGED from “No Diagnosis” to “Encounter for observation for other suspected diseases and conditions ruled out.” established. October 1, 2019, with the 2020 edition of ICD-10-CM.
For claims for screening for syphilis in pregnant women at increased risk for STIs use the following ICD-10-CM diagnosis codes: • Z11. 3 - Encounter for screening for infections with a predominantly sexual mode of transmission; • and any of: Z72.
Hereditary spherocytosis is characterized by hemolysis of spheroidal RBCs and anemia. Hereditary elliptocytosis (ovalocytosis) is a rare autosomal dominant disorder in which RBCs are oval or elliptical.
Elliptocytes are elongated oval-shaped red blood cells. Very rare elliptocytes may be seen in normal blood smears. Elliptocytes may be increased in iron deficiency anemia (where they are sometimes referred to as “pencil cells”) and marrow infiltrative processes (with teardrop cells).
Elliptocytes: Red blood cells are cigar or pencil shaped with parallel sides and an area of pallor. Ovalocytes: Are red blood cells that are oval or egg shaped.
Approach Considerations. In most cases, hereditary elliptocytosis (HE) causes no symptoms and requires no therapy. For patients with clinically significant hemolytic anemia, splenectomy provides marked improvement.
Heinz bodies may be present in patients with glucose-6-phosphate dehydrogenase (G6PD), or FAD f(adenine dinucleotide deficiency), i.e. methemoglobinemia. [6] it may also indicate unstable hemoglobin, e.g. HB Koln.
Elliptocytosis affects about 1 in every 2,500 people of northern European heritage. It is more common in people of African and Mediterranean descent. You are more likely to develop this condition if someone in your family has had it.
How Is Pancytopenia Diagnosed?A complete blood count, which tells how many blood cells you have of each type.A peripheral blood smear, which is when a sample of your blood is examined under a microscope.A check of your vitamin B12 and folate levels.Tests to check your liver function.Tests for infectious diseases.More items...•
The 2022 edition of ICD-10-CM D58.0 became effective on October 1, 2021.
An autosomal dominant inherited disorder characterized by the presence of smaller than normal, sphere-shaped erythrocytes. It results in hemolytic anemia and splenomegaly.
A familial congenital hemolytic anemia characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.
The 2022 edition of ICD-10-CM Z86.718 became effective on October 1, 2021.
Z77-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status
Personal history of other diseases of the female genital tract 1 Z87.42 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 Short description: Personal history of oth diseases of the female genital tract 3 The 2021 edition of ICD-10-CM Z87.42 became effective on October 1, 2020. 4 This is the American ICD-10-CM version of Z87.42 - other international versions of ICD-10 Z87.42 may differ.
The 2022 edition of ICD-10-CM Z87.42 became effective on October 1, 2021.