WebID: http://purl.bioontology.org/ontology/ICD10CM/E70.0. cui: C0751434. notation: E70.0. Order number: 04650. prefLabel: Classical phenylketonuria. tui: T047. subClassOf WebCode History. E70.1 is a billable ICD-10 code used to specify a medical diagnosis of other hyperphenylalaninemias. The code is valid during the fiscal year 2024 from October 01, 2024 through September 30, 2024 for the submission of HIPAA-covered transactions.
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WebMay 20, 2024 · D68.2 Hereditary deficiency of other clotting factors 0-64 1, 2-F, 3 E70.0 Classical phenylketonuria 0-20 1, 2E, 3 E70.1 Other hyperphenylalaninemias 0-20 1, 2E, 3 E70.20 Disorder of tyrosine metabolism, unspecified 0-20 1, 2E, 3 E70.21 Tyrosinemia 0-20 1, 2E, 3 E70.29 Other disorders of tyrosine metabolism 0-20 1, 2E, 3 Web270.1. Phenylketonuria [PKU] (approximate match) This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping … how to remove spn from user account
ICD-10-CM Code for Classical phenylketonuria E70.0 - AAPC
WebE70.0 Classical phenylketonuria E70.21 Tyrosinemia E71.0 Maple Syrup Urine Disease E71.110 Isovaleric acidemia E71.111 3-methylglutaconic aciduria E71.120 Methylmalonic acidemia E71.121 Propionic acidemia E71.310 LCAD/LCHAD/VLCAD Fatty acid oxidation disorders and ketogenesis disorders E71.311 MCAD Fatty acid oxidation disorders and … WebOct 1, 2024 · E70.0 Classical phenylketonuria E70.1 Other hyperphenylalaninemias E70.2 Disorders of tyrosine metabolism E70.20 Disorder of tyrosine metabolism, unspecified; E70.21 Tyrosinemia. Inclusion term(s): Hypertyrosinemia; E70.29 Other disorders of tyrosine metabolism. Inclusion term(s): Alkaptonuria; Ochronosis; E70.3 Albinism E70.30 Albinism ... WebDec 19, 2008 · Phenylketonuria is an inherited disorder that increases levels of the amino acid phenylalanine in the blood. Infants with classic PKU appear normal until … how to remove spn