Classical phenylketonuria. E70.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Z13.228 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 Z13.228 became effective on October 1, 2018. This is the American ICD-10-CM version of Z13.228 - other international versions of ICD-10 Z13.228 may differ.
E70.1 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 E70.1 became effective on October 1, 2019. This is the American ICD-10-CM version of E70.1 - other international versions of ICD-10 E70.1 may differ.
E70.0 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 E70.0 became effective on October 1, 2018. This is the American ICD-10-CM version of E70.0 - other international versions of ICD-10 E70.0 may differ.
"Z14. 8 - Genetic Carrier of Other Disease." ICD-10-CM, 10th ed., Centers for Medicare and Medicaid Services and the National Center for Health Statistics, 2018.
D56. 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 D56. 0 became effective on October 1, 2021.
Names and CodesCondition:1PhenylketonuriaCategory:2CoreSNOMED CT Code:37573000—Classical phenylketonuria UMLS CUI:4C0751434ICD-9-CM Code:5270.1—Phenylketonuria [PKU]ICD-10-CM Code:6E70.0—Classical phenylketonuria1 more row
Z13. 228 - Encounter for screening for other metabolic disorders | ICD-10-CM.
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.
A carrier of thalassaemia is someone who carries at least 1 of the faulty genes that causes thalassaemia, but does not have thalassaemia themselves. It's also known as having the thalassaemia trait. If you're a thalassaemia carrier, you will not develop thalassaemia.
Listen to pronunciation. (FEH-nil-KEE-tone-yoor-ee-uh) An inherited disorder that causes a build-up of phenylalanine (an amino acid) in the blood. This can cause mental retardation, behavioral and movement problems, seizures, and delayed development.
HCPCS code S3620 for Newborn metabolic screening panel, includes test kit, postage and the laboratory tests specified by the state for inclusion in this panel (e.g., galactose; hemoglobin, electrophoresis; hydroxyprogesterone, 17-D; phenylanine (PKU); and thyroxine, total) as maintained by CMS falls under Miscellaneous ...
Background. Hyperphenylalaninemia is a hereditary metabolic disorder that causes elevated blood phenylalanine (Phe). Hyperphenylalaninemias are classified as Phenylketonuria PKU (Phe > 6 mg/dL) or mild hyperphenylalaninemia (mHPA) (Phe 2–6 mg/dL).
Group 1CodeDescription80047Metabolic panel ionized ca80048Metabolic panel total ca80051Electrolyte panel80053Comprehen metabolic panel3 more rows•Nov 21, 2019
82947 is included in the BMP code. You should be using 80048 for your BMP code and that it is it. You would not separately bill out 82947.
ICD-10 Code for Encounter for newborn, infant and child health examinations- Z00. 1- Codify by AAPC.