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ALL MEDICAL CODES IN CATEGORY Chromosomal abnormalities, not elsewhere classified

2025 ICD-10-CM code Q91

Trisomy 18 and Trisomy 13

2025 ICD-10-CM code Q99.9

This code represents an unspecified chromosomal abnormality.

2025 ICD-10-CM code Q90

Down syndrome, a chromosomal abnormality characterized by an extra copy of chromosome 21.

2025 ICD-10-CM code Q93.81

Velo-cardio-facial syndrome, a chromosomal abnormality.

2025 ICD-10-CM code Q91.2

Trisomy 18, translocation.

2025 ICD-10-CM code Q95

Balanced rearrangements and structural markers, not elsewhere classified. Includes: Robertsonian and balanced reciprocal translocations and insertions.

2025 ICD-10-CM code Q91.4

Trisomy 13, nonmosaicism (meiotic nondisjunction)

2025 ICD-10-CM code Q93.5

This code represents other deletions of part of a chromosome.

2025 ICD-10-CM code Q96.2

Karyotype 46,X with abnormal sex chromosome, except isochromosome Xq.

2025 ICD-10-CM code Q90.0

Trisomy 21, nonmosaicism (meiotic nondisjunction). This condition is characterized by the presence of an extra copy of chromosome 21, specifically due to meiotic nondisjunction.

2025 ICD-10-CM code Q98.5

Karyotype 47, XYY is a chromosomal abnormality characterized by an extra Y chromosome.

2025 ICD-10-CM code Q96.3

This ICD-10 code represents Mosaicism, a condition where an individual has two or more cell populations with different chromosomal compositions, specifically 45,X/46,XX or XY.

2025 ICD-10-CM code Q96.9

Turner's syndrome, unspecified.

2025 ICD-10-CM code Q97.0

Karyotype 47, XXX. This code represents the presence of an extra X chromosome in females, resulting in a 47,XXX karyotype.

2025 ICD-10-CM code Q97.1

Female with more than three X chromosomes.

2025 ICD-10-CM code Q95.0

Balanced translocation and insertion in a normal individual.

2025 ICD-10-CM code Q95.3

This code represents a balanced sex/autosomal rearrangement in an abnormal individual.

2025 ICD-10-CM code Q95.5

Individual with autosomal fragile site.

2025 ICD-10-CM code Q95.8

Other balanced rearrangements and structural markers. This code encompasses chromosomal abnormalities that are balanced and not classified elsewhere.

2025 ICD-10-CM code Q98.8

Other specified sex chromosome abnormalities, male phenotype.

2025 ICD-10-CM code Q99.2

Fragile X chromosome; a genetic condition causing intellectual disability.

2025 ICD-10-CM code Q95.2

Balanced autosomal rearrangement in an abnormal individual.

2025 ICD-10-CM code Q95.9

Balanced rearrangement and structural marker, unspecified.

2025 ICD-10-CM code Q96.1

Karyotype 46, isochromosome Xq.

2025 ICD-10-CM code Q96

Turner syndrome, a chromosomal disorder characterized by the absence of all or part of one X chromosome in females.

2025 ICD-10-CM code Q92.9

Trisomy and partial trisomy of autosomes, unspecified.

2025 ICD-10-CM code Q90.9

Down syndrome, unspecified; Trisomy 21 NOS.

2025 ICD-10-CM code Q92.8

Other specified trisomies and partial trisomies of autosomes.

2025 ICD-10-CM code Q99.9

이 코드는 지정되지 않은 염색체 이상을 나타냅니다.

2025 ICD-10-CM code Q99.9

يمثل هذا الرمز شذوذًا كروموسوميًا غير محدد.

2025 ICD-10-CM code Q99.9

该代码代表未指明的染色体异常。

2025 ICD-10-CM code Q99.9

Этот код представляет собой неуточненную хромосомную аномалию.

2025 ICD-10-CM code Q99.9

Este código representa una anomalía cromosómica no especificada.

2025 ICD-10-CM code Q99.9

Ce code représente une anomalie chromosomique non spécifiée.

2025 ICD-10-CM code Q99.9

Ang code na ito ay kumakatawan sa isang hindi tinukoy na anomalidad ng kromosomal.

2025 ICD-10-CM code Q99.9

Mã này đại diện cho một bất thường nhiễm sắc thể không xác định.

2025 ICD-10-CM code Q99.9

Dieser Code steht für eine nicht näher bezeichnete Chromosomenanomalie.

2025 ICD-10-CM code Q98.4

Klinefelter syndrome, unspecified.

2025 ICD-10-CM code Q93.88

This code represents other microdeletions, including Miller-Dieker syndrome and Smith-Magenis syndrome.

2025 ICD-10-CM code Q92.6

Marker chromosomes.This condition involves the presence of extra marker chromosomes in an individual's genetic makeup.

2025 ICD-10-CM code Q91.1

Trisomy 18, mosaicism (mitotic nondisjunction).

2025 ICD-10-CM code Q93.82

Williams syndrome, a genetic disorder.

2025 ICD-10-CM code Q98.0

Klinefelter syndrome karyotype 47, XXY.

2025 ICD-10-CM code Q98.4

克林费尔特综合症，未指明。

2025 ICD-10-CM code Q98.5

핵형 47, <a href="../medical-coding/reference/XYY" target="_blank" title="Medical Code XYY 2025">XYY는 여분의 Y</a> 염색체를 특징으로 하는 염색체 이상입니다.

2025 ICD-10-CM code Q99.2

Chromosome X fragile ; maladie génétique à l'origine d'une déficience intellectuelle.

2025 ICD-10-CM code Q99.2

Marupok na kromosoma X; isang kondisyong henetiko na nagdudulot ng kapansan

2025 ICD-10-CM code Q99.2

Nhiễm sắc thể X mỏng manh; một tình trạng di truyền gây ra khuyết tật trí tuệ.

2025 ICD-10-CM code Q99.2

脆弱的 X 染色体；一种导致智力障碍的遗传疾病。

2025 ICD-10-CM code Q96.8

Другие варианты синдрома Тернера.