Maternal care for (suspected) chromosomal abnormality in fetus, not applicable or unspecified. O35.1XX0 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 O35.1XX0 became effective on October 1, 2018.
2021 ICD-10-CM Codes Q00-Q99: Congenital malformations, deformations and chromosomal abnormalities ICD-10-CM Codes
Short description: Maternal care for fetal abnormality and damage, unsp, unsp The 2020 edition of ICD-10-CM O35.9XX0 became effective on October 1, 2019. This is the American ICD-10-CM version of O35.9XX0 - other international versions of ICD-10 O35.9XX0 may differ.
2019 ICD-10-CM Diagnosis Code O35.9XX0 Maternal care for (suspected) fetal abnormality and damage, unspecified, not applicable or unspecified Billable/Specific Code Maternity Dx (12-55 years) Female Dx ICD-10-CM Coding Rules O35.9XX0 is applicable to maternity patients aged 12 - 55 years inclusive. O35.9XX0 is applicable to female patients.
Encounter for supervision of normal pregnancy, unspecified90 Encounter for supervision of normal pregnancy, unspecified, unspecified trimester.
ICD-10 code Z15. 89 for Genetic susceptibility to other disease is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .
Chromosomal abnormality, unspecified Q99. 9 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 Q99. 9 became effective on October 1, 2021.
ICD-10 Code for Encounter for other screening for genetic and chromosomal anomalies- Z13. 79- Codify by AAPC.
Ankylosing spondylitis of unspecified sites in spine The 2022 edition of ICD-10-CM M45. 9 became effective on October 1, 2021. This is the American ICD-10-CM version of M45.
315.9 - Unspecified delay in development | ICD-10-CM.
MUTYH (mutY DNA glycosylase) is a human gene that encodes a DNA glycosylase, MUTYH glycosylase. It is involved in oxidative DNA damage repair and is part of the base excision repair pathway.
Codes from category Z15 should not be used as principal or first-listed codes.
TBCK (TBC1 Domain Containing Kinase) is the name of a gene. This gene codes for a protein of the same name. This protein helps to regulate signals along the mTOR pathway in cells. The mTOR pathway is a key regulator of cell metabolism, growth, proliferation, and survival.
A chromosomal anomaly is a change to a child's genetic material or DNA, which alters the baby's development before birth. This can include extra, missing or irregular chromosomes.
What are aneuploidy screening tests? Screening tests give information about your baby's risk of a chromosome disorder. This testing is optional, and not all pregnant women have it. Some of these tests also screen for problems with your baby's brain or spine.
Some chromosomal abnormalities occur when there is an extra chromosome, while others occur when a section of a chromosome is deleted or duplicated. Examples of chromosomal abnormalities include Down syndrome, Trisomy 18, Trisomy 13, Klinefelter syndrome, XYY syndrome, Turner syndrome and triple X syndrome.
the listed conditions in the fetus as a reason for hospitalization or other obstetric care to the mother, or for termination of pregnancy
NEC Not elsewhere classifiable This abbreviation in the Tabular List represents “other specified”. When a specific code is not available for a condition, the Tabular List includes an NEC entry under a code to identify the code as the “other specified” code.