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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 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 Q92.1

Whole chromosome trisomy, mosaicism (mitotic nondisjunction).

2025 ICD-10-CM code Q92.7

Triploidy and polyploidy are chromosomal abnormalities involving an extra set or sets of chromosomes.

2025 ICD-10-CM code Q96.0

Karyotype 45, X, also known as Turner syndrome, is a chromosomal abnormality characterized by the absence of one X chromosome in females.

2025 ICD-10-CM code Q96.8

Other variants of Turner syndrome.

2025 ICD-10-CM code Q92.62

Marker chromosomes in an abnormal individual.

2025 ICD-10-CM code Q99

Other chromosome abnormalities not specified elsewhere.

2025 ICD-10-CM code Q91.3

Trisomy 18, unspecified.

2025 ICD-10-CM code Q99.9

이 코드는 지정되지 않은 염색체 이상을 나타냅니다.

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 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 Q90.1

Trisomy 21, mosaicism (mitotic nondisjunction).

2025 ICD-10-CM code Q93.3

Suppression du bras court du chromosome 4 (syndrome de Wolff-Hirschorn).

2025 ICD-10-CM code Q93.4

Удаление короткого плеча хромосомы 5, также известное как синдром Кри-дю-Чата.

2025 ICD-10-CM code Q93.4

Suppression du bras court du chromosome 5, également connue sous le nom de syndrome de Cri-du-Chat.

2025 ICD-10-CM code Q93.82

Синдром Уильямса, генетическое заболевание.

2025 ICD-10-CM code Q93.88

Ce code représente d'autres microdélétions, notamment le syndrome de Miller-Dieker et le syndrome de Smith-Magenis.

2025 ICD-10-CM code Q93.88

이 코드는 밀러-디커 증후군 및 스미스-마게니스 증후군을 비롯한 다른 미세 결실을 나타냅니다.

2025 ICD-10-CM code Q93.88

Este código representa otras microdeleciones, como el síndrome de Miller-Dieker y el síndrome de Smith-Magenis.

2025 ICD-10-CM code Q93.82

윌리엄스 증후군, 유전 질환.

2025 ICD-10-CM code Q93.4

缺失5号染色体的短臂,也称为Cri-du-Chat综合征。

2025 ICD-10-CM code Q93.4

حذف الذراع القصيرة للكروموسوم 5، المعروف أيضًا باسم متلازمة Cri-du-chat.

2025 ICD-10-CM code Q93.4

Deletion des kurzen Arms von Chromosom 5, auch bekannt als Cri-du-Chat-Syndrom.

2025 ICD-10-CM code Q93.82

Síndrome de Williams, un trastorno genético.

2025 ICD-10-CM code Q93.8

Các trường hợp xóa khác khỏi các autosome. Điều này cho thấy một mảnh nhiễm sắc thể bị thiếu.

2025 ICD-10-CM code Q93.8

Otras eliminaciones de los autosomas. Esto indica que falta una parte de un cromosoma.