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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 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 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 Q92
Other trisomies and partial trisomies of the autosomes, not elsewhere classified. Includes unbalanced translocations and insertions.
Mosaicism, lines with various numbers of X chromosomes.This is a congenital disorder involving variations in the number of X chromosomes across different cells in the body.
2025 ICD-10-CM code Q93.4
Deletion of the short arm of chromosome 5, also known as Cri-du-chat syndrome.
2025 ICD-10-CM code Q93.51
Angelman syndrome, a rare neuro-genetic disorder characterized by developmental delays, intellectual disability, speech impairment, movement and balance problems, and a happy demeanor.
2025 ICD-10-CM code Q93.7
Deletions with other complex rearrangements.This code describes chromosomal deletions occurring alongside other complex chromosomal changes.
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 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 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.
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