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ALL MEDICAL CODES IN CATEGORY Q90-Q99

2025 ICD-10-CM code Q91.5

Trisomy 13, mosaicism (mitotic nondisjunction).

2025 ICD-10-CM code Q91.7

Trisomy 13, unspecified.

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 Q98.8

Other specified sex chromosome abnormalities, male phenotype.

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 Q98.1

Klinefelter syndrome, male with more than two X chromosomes.

2025 ICD-10-CM code Q97.8

Other specified sex chromosome abnormalities, female phenotype.

2025 ICD-10-CM code Q98.4

Klinefelter syndrome, unspecified.

2025 ICD-10-CM code Q93.3

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

2025 ICD-10-CM code Q99.8

Other specified chromosome abnormalities.

2025 ICD-10-CM code Q95.5

Individual with autosomal fragile site.

2025 ICD-10-CM code Q91.2

Trisomy 18, translocation.

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 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 Q95

Balanced rearrangements and structural markers, not elsewhere classified. Includes: Robertsonian and balanced reciprocal translocations and insertions.

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 Q91.4

Trisomy 13, nonmosaicism (meiotic nondisjunction)

2025 ICD-10-CM code Q95.3

This code represents a balanced sex/autosomal rearrangement in an abnormal individual.

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 Q96.2

Karyotype 46,X with abnormal sex chromosome, except isochromosome Xq.

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 Q93

Monosomies and deletions from the autosomes, not elsewhere classified.

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 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 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 Q93.0

Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction).

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 Q92.6

Marker chromosomes.This condition involves the presence of extra marker chromosomes in an individual's genetic makeup.

2025 ICD-10-CM code Q92

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