icd 10 code for anomaly chromosome x

Full Answer

What is the ICD 10 code for chromosomal abnormalities?

Other specified chromosome abnormalities. Q99.8 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 Q99.8 became effective on October 1, 2020.

What are the different types of chromosome abnormalities?

Other specified chromosome abnormalities 1 Autosomal aneuploidy. 2 Unbalanced chromosomal translocation (abnormal structure of chromosomes). 3 Unbalanced translocation of chromosome. 4 Undervirilization of male due to steroidogenic acute regulatory protein deficiency. 5 Undervirilized xy, star protein deficiency. 6 ... (more items)

What is fragile X chromosome?

Fragile X chromosome. It is a common cause of mental retardation, second only in frequency to the down syndrome (trisomy 21). The expression varies with mental retardation, macroorchidism, high-pitched voice, narrow face, long jaw, large ears, prominent forehead, highly arched narrow palate, and joint laxity as the most common characteristics.

What is a chromosome anomaly?

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 is the code for fragile X syndrome?

ICD-10-CM Code for Fragile X chromosome Q99. 2.

What is the ICD-10 code for congenital anomalies?

If coded, the ICD-10 code is Q89. 9 (Congenital malformation, unspecified).

What is diagnosis code Z13 79?

ICD-10 code Z13. 79 for Encounter for other screening for genetic and chromosomal anomalies is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .

What are the congenital anomaly codes?

Coding Clinic has advised to assign code 759.89, Other specified anomalies, on several occasions for congenital syndromes that are not indexed to a specific code. Also in several instances, the ICD-9-CM index will direct the coder to code 759.89 for some congenital anomalies.

What are multiple congenital anomalies?

Multiple congenital anomaly is the occurrence of two or more major anomalies that are unrelated. This means that the major anomalies are presumed to be a random association, and do not constitute a sequence or a previously recognized syndrome.

Which codes are used to describe congenital problems?

Q00-Q07 Congenital malformations of the nervous system • Q10-Q18 Congenital malformations of eye, ear, face and neck • Q20-Q28 Congenital malformations of the circulatory system • Q30-Q34 Congenital malformations of the respiratory system • Q35-Q37 Cleft lip and cleft palate • Q38-Q45 Other congenital malformations of ...

What is procedure code 81420?

CPT® 81420, Under Genomic Sequencing Procedures and Other Molecular Multianalyte Assays. The Current Procedural Terminology (CPT®) code 81420 as maintained by American Medical Association, is a medical procedural code under the range - Genomic Sequencing Procedures and Other Molecular Multianalyte Assays.

What is Encounter for antenatal screening for chromosomal anomalies?

Encounter for antenatal screening of mother Screening is the testing for disease or disease precursors in asymptomatic individuals so that early detection and treatment can be provided for those who test positive for the disease.

What is the ICD-10 code for genetic mutation?

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.

What is a mutation of the distal end of the long arm of the X chromosome?

A condition characterized genotypically by mutation of the distal end of the long arm of the x chromosome (at gene loci fraxa or fraxe) and phenotypically by cognitive impairment, hyperactivity, seizures, language delay, and enlargement of the ears, head, and testes.

What is fragile x syndrome?

Fragile x syndrome is the most common form of inherited mental retardation. A problem with a specific gene causes the disease. Normally, the gene makes a protein you need for brain development. But the mutation causes a person to make little or none of the protein, which results in the symptoms of fragile x.

What is the genetic cause of mental retardation?

A genetic syndrome caused by mutations in the fmr1 gene which is responsible for the expression of the fragile x mental retardation 1 protein. This protein participates in neural development. This syndrome is manifested with mental, emotional, behavioral, physical, and learning disabilities. An inherited disease characterized by the presence ...