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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 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.
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 Q90.1
Trisomy 21, mosaicism (mitotic nondisjunction).
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 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 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.
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