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ALL MEDICAL CODES IN CATEGORY Q90-Q99

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 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 Q97.8

Other specified sex chromosome abnormalities, female phenotype.

2025 ICD-10-CM code Q98.1

Klinefelter syndrome, male with more than two X chromosomes.

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 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 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 Q99.0

Chimera 46, XX/46, XY. This condition represents a rare genetic abnormality where an individual has two distinct cell lines, one with a female (46, XX) and one with a male (46, XY) karyotype.

2025 ICD-10-CM code Q93.3

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

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.

2025 ICD-10-CM code Q93.0

Monosomía cromosómica completa, no mosaicismo (no disyunción meiótica).

2025 ICD-10-CM code Q93.8

常染色体中的其他删除。这表明一条染色体缺失了一部分。

2025 ICD-10-CM code Q93.8

Andere Deletionen aus den Autosomen. Dies deutet auf ein fehlendes Stück eines Chromosoms hin.

2025 ICD-10-CM code Q93.8

Autres délétions des autosomes. Cela indique un fragment manquant d'un chromosome.

2025 ICD-10-CM code Q93.8

상염색체에서의 기타 삭제.이는 염색체의 누락된 부분을 나타냅니다.

2025 ICD-10-CM code Q93.8

Iba pang mga pagtanggal mula sa mga autosome. Ipinapahiwatig nito ang isang nawawalang piraso ng isang kromosoma.

2025 ICD-10-CM code Q93

Monosomien und Deletionen aus den Autosomen, nicht anderweitig klassifiziert.

2025 ICD-10-CM code Q93.3

4号染色体短臂缺失（沃尔夫-赫舍恩综合症）。

2025 ICD-10-CM code Q93.3

Deletion des kurzen Arms von Chromosom 4 (Wolff-Hirschorn-Syndrom).

2025 ICD-10-CM code Q92.61

Cromosomas marcadores en individuos normales. Esta afección implica la presencia de pequeños cromosomas adicionales denominados cromosomas marcadores, que suelen presentarse en personas con un fenotipo normal.

2025 ICD-10-CM code Q93.3

Xóa nhánh ngắn của nhiễm sắc thể 4 (hội chứng Wolff-Hirschorn).

2025 ICD-10-CM code Q93.2

Cromosoma reemplazado por anillo, dicéntrico o isocromosoma. Esta afección implica un cambio estructural en el que los segmentos de uno o más autosomas se rompen y se reorganizan, lo que lleva a la formación de un anillo, un dicéntrico o un isocromosoma.

2025 ICD-10-CM code Q93.3

염색체 4의 단팔 결실 (볼프-허쇼른 증후군).

2025 ICD-10-CM code Q93.2

染色体被环状、双中心或等染色体所取代。这种情况涉及结构变化，其中一个或多个常染色体的片段被破坏并重新排列，从而形成环状、双中心或同染色体。

2025 ICD-10-CM code Q93.2

Nhiễm sắc thể được thay thế bằng vòng, dicentric hoặc isochromosome. Tình trạng này liên quan đến sự thay đổi cấu trúc trong đó các đoạn của một hoặc nhiều autosome bị phá vỡ và sắp xếp lại, dẫn đến hình thành vòng, phân tâm hoặc isochromosome.

2025 ICD-10-CM code Q99.8

Other specified chromosome abnormalities.

2025 ICD-10-CM code Q90.2

Trisomy 21, translocation. This condition is characterized by an extra copy of chromosome 21 material.It is often familial, commonly involving chromosomes 14 and 21.

2025 ICD-10-CM code Q92.61

Marker chromosomes in normal individual. This condition involves the presence of small, extra chromosomes called marker chromosomes, which are typically seen in individuals with a normal phenotype.

2025 ICD-10-CM code Q93

Monosomies and deletions from the autosomes, not elsewhere classified.

2025 ICD-10-CM code Q93.0

Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction).

2025 ICD-10-CM code Q93.2

Chromosome replaced with ring, dicentric or isochromosome. This condition involves a structural change where segments of one or more autosomes are broken and rearranged, leading to a ring, dicentric, or isochromosome formation.

2025 ICD-10-CM code Q93.3

Deletion of short arm of chromosome 4 (Wolff-Hirschorn syndrome).

2025 ICD-10-CM code Q91.5

Trisomy 13, mosaicism (mitotic nondisjunction).

2025 ICD-10-CM code Q91.6

Trisomy 13, translocation. This is a congenital disorder where there are three copies of chromosome 13 instead of the usual two, due to a translocation.

2025 ICD-10-CM code Q91.7

Trisomy 13, unspecified.

2025 ICD-10-CM code Q92

Other trisomies and partial trisomies of the autosomes, not elsewhere classified. Includes unbalanced translocations and insertions.

2025 ICD-10-CM code Q93.8

Other deletions from the autosomes. This indicates a missing piece of a chromosome.

2025 ICD-10-CM code Q98.4

克林费尔特综合症，未指明。

2025 ICD-10-CM code Q99.0

<a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">Chimère 46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a> /46, XY.</a> Cette affection représente une anomalie génétique rare lorsqu'un individu possède deux lignées cellulaires distinctes, l'une avec un caryotype féminin (46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a>) et l'autre avec un caryotype masculin (46, <a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">XY</a>).

2025 ICD-10-CM code Q98.4

Hội chứng Klinefelter, không xác định.

2025 ICD-10-CM code Q99.0

<a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">Quimera 46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX/46</a>, XY.</a> Esta afección representa una anomalía genética poco frecuente en la que un individuo tiene dos líneas celulares distintas, una con un cariotipo femenino (46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a>) y otra con un cariotipo masculino (46, <a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">XY</a>).

2025 ICD-10-CM code Q99.0

<a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">Chimäre 46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a> /46, XY.</a> Diese Erkrankung stellt eine seltene genetische Abnormalität dar, bei der ein Individuum zwei verschiedene Zelllinien hat, eine mit einem weiblichen (46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a>) und eine mit einem männlichen (46, <a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">XY</a>) Karyotyp.

2025 ICD-10-CM code Q99.0

<a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">키메라 46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a> /46, XY.</a><a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">이 질환은 개체가 서로 다른 두 개의 세포주, 즉 암컷 (46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX) 과 수컷 (46, XY</a>) 핵형을 갖는 드문 유전적 이상을 나타냅니다.</a>