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Marker chromosomes.This condition involves the presence of extra marker chromosomes in an individual's genetic makeup.
2025 ICD-10-CM code Q98.3
This code represents a male individual with a 46, XX karyotype, a condition where a male has two X chromosomes instead of one X and one Y chromosome.
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 Q99.8
Autres anomalies chromosomiques précisées.
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.
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 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 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>
2025 ICD-10-CM code Q99.0
<a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">Chimera 46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a> /46, XY.</a> Tình trạng này thể hiện một bất thường di truyền hiếm gặp trong đó một cá thể có hai dòng tế bào riêng biệt, một dòng có nữ (46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a>) và một dòng có karyotype nam (46, <a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">XY</a>).
<a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">Chimera 46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a> /46, XY.</a> Ang kondisyong ito ay kumakatawan sa isang bihirang anomaliyang henetiko kung saan ang isang indibidwal ay may dalawang natatanging mga linya ng cell, isa na may babae (46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a>) at isa na may isang lalaking (46, <a href="../medical-coding/reference/XY" target="_blank" title="Medical Code XY 2025">XY</a>) karyotype.
2025 ICD-10-CM code Q98.8
Autres anomalies des chromosomes sexuels précisées, phénotype masculin.
2025 ICD-10-CM code Q98.8
其他特定的性染色体异常，男性表型。
2025 ICD-10-CM code Q98.8
Otras anomalías cromosómicas sexuales especificadas, fenotipo masculino.
2025 ICD-10-CM code Q98.8
Các bất thường nhiễm sắc thể giới tính được chỉ định khác, kiểu hình nam.
2025 ICD-10-CM code Q98.8
Andere näher bezeichnete Geschlechtschromosomenanomalien, männlicher Phänotyp.
2025 ICD-10-CM code Q98.8
기타 특정 성염색체 이상, 남성 표현형.
2025 ICD-10-CM code Q98.8
Iba pang tinukoy na mga anomalidad sa kromosoma ng kasarian, phenotype ng lalaki
2025 ICD-10-CM code Q98.4
Klinefelter-Syndrom, nicht näher bezeichnet.
2025 ICD-10-CM code Q97.8
其他特定的性染色体异常，女性表型。
2025 ICD-10-CM code Q98.4
Síndrome de Klinefelter, no especificado.
2025 ICD-10-CM code Q98.3
该代码代表具有46，<a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a> 核型的男性个体，在这种情况下，雄性有两条X染色体，而不是一条X和一条Y染色体。
2025 ICD-10-CM code Q98.3
Este código representa a un individuo masculino con un cariotipo 46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a>, una afección en la que un hombre tiene dos cromosomas X en lugar de un cromosoma X y un cromosoma Y.
2025 ICD-10-CM code Q98.4
클라인펠터 증후군, 상세불명
2025 ICD-10-CM code Q98.3
Dieser Code steht für ein männliches Individuum mit einem <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">46,XX-Karyotyp</a>, einer Erkrankung, bei der ein Männchen zwei X-Chromosomen anstelle eines X- und eines Y-Chromosoms hat.
2025 ICD-10-CM code Q98.1
Syndrome de Klinefelter, homme avec plus de deux chromosomes X.
2025 ICD-10-CM code Q98.3
Ce code représente un individu de sexe masculin présentant un caryotype 46, <a href="../medical-coding/reference/XX" target="_blank" title="Medical Code XX 2025">XX</a>, une affection dans laquelle un homme possède deux chromosomes X au lieu d'un chromosome X et d'un chromosome Y.
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