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For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes). ICD-10-CM Code for Trisomy 18, translocation Q91.2 ICD-10 code Q91.2 for Trisomy 18, translocation is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities . ICD-10-CM Code for Trisomy 21, translocation Q90.2 ICD-10 code Q90.2 for Trisomy 21, translocation is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities . Patau syndrome is a syndrome caused by a chromosomal abnormality, in which some or all of the cells of the body contain extra genetic material from chromosome 13.The extra genetic material disrupts normal development, causing multiple and complex organ defects. This can occur either because each cell contains a full extra copy of chromosome 13 (a disorder known as trisomy 13 or trisomy D or Create codetable from scratch Show conversion to ICD-9-CM Contact.

ICD-10-CM Diagnosis Code Q92.8. Other specified trisomies and partial trisomies of autosomes. Trisomy and partial trisomy of autosomes, unspecified 2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt Q92.9 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 Q92.9 became effective on October 1, 2020. | ICD-10 from 2011 - 2016 Q92.8 is a billable ICD code used to specify a diagnosis of other specified trisomies and partial trisomies of autosomes. A 'billable code' is detailed enough to be used to specify a medical diagnosis.

Health examination for newborn under 8 days old. ICD-10-CM Diagnosis Code Q92.8. Other specified trisomies and partial trisomies of autosomes.

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Kapitel XVII Angeborene Fehlbildungen, Deformitäten und Chromosomenanomalien (Q00-Q99) Trisomie der Chromosomen 13, 18, 21 . Create codetable from scratch Show conversion to ICD-9-CM Contact. Syndrome --see also Disease trisomy Q92.9 13 Q91.7 meiotic nondisjunction Q91.4 mitotic nondisjunction Q91.5 mosaicism Q91.5 translocation Q91.6 18 Q91.3 meiotic nondisjunction Q91.0 mitotic nondisjunction Q91.1 mosaicism Q91.1 translocation Q91.2 20 (q)(p) Q92.8 21 Q90.9 meiotic nondisjunction Q90.0 mitotic nondisjunction Q90 ICD-10-CM Code for Trisomy 18, translocation Q91.2 ICD-10 code Q91.2 for Trisomy 18, translocation is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .

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ICD-10 is the 10th revision of the International Statistical Classification of Diseases and Related Health Problems (ICD), a medical classification list by the World Health Organization (WHO). It contains codes for diseases, signs and symptoms, abnormal findings, complaints, social circumstances, and external causes of injury or diseases.
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May 12, 2017 Page 1 of 10. CLINICAL aneuploidy as screening tools for trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), or ICD-10 Codes Description O28.8. Other abnormal findings on antenatal screening of mother&n Oct 22, 2019 1st Column called 'ICD-10' – ICD-10 codes that correspond to the child's birth defect. Q04.8. Other specified congenital malformation of brain (must specify) Edwards syndrome, karyotype trisomy 18(47,X ICD-10-CM Official Guidelines for Coding and Reporting.

(author); The policy orientation : legacy and Trisomy 12 was identified as a recurrent and sometimes early event in breast carcinogenesis.
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Suchergebnisse 1 - 4 von 4. Q92.-. Sonstige Trisomien und partielle Trisomien der Autosomen, anderenorts nicht klassifiziert. Q92.-.