VITiếng Việt
ICD-10 Vietnam

Q90-Q99

Chromosomal abnormalities, not elsewhere classified

Q96.4 Primary diagnosis candidate Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome Q96.8 Primary diagnosis candidate Other variants of Turner syndrome Q96.9 Primary diagnosis candidate Turner syndrome, unspecified Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified Q97.0 Primary diagnosis candidate Karyotype 47,XXX Q97.1 Primary diagnosis candidate Female with more than three X chromosomes Q97.2 Primary diagnosis candidate Mosaicism, lines with various numbers of X chromosomes Q97.3 Primary diagnosis candidate Female with 46,XY karyotype Q97.8 Primary diagnosis candidate Other specified sex chromosome abnormalities, female phenotype Q97.9 Primary diagnosis candidate Sex chromosome abnormality, female phenotype, unspecified Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified Q98.0 Primary diagnosis candidate Klinefelter syndrome karyotype 47,XXY Q98.1 Primary diagnosis candidate Klinefelter syndrome, male with more than two X chromosomes Q98.2 Primary diagnosis candidate Klinefelter syndrome, male with 46,XX karyotype Q98.3 Primary diagnosis candidate Other male with 46,XX karyotype Q98.4 Primary diagnosis candidate Klinefelter syndrome, unspecified Q98.5 Primary diagnosis candidate Karyotype 47,XYY Q98.6 Primary diagnosis candidate Male with structurally abnormal sex chromosome Q98.7 Primary diagnosis candidate Male with sex chromosome mosaicism Q98.8 Primary diagnosis candidate Other specified sex chromosome abnormalities, male phenotype Q98.9 Primary diagnosis candidate Sex chromosome abnormality, male phenotype, unspecified Q99 Other chromosome abnormalities, not elsewhere classified Q99.0 Primary diagnosis candidate Chimera 46,XX/46,XY Q99.1 Primary diagnosis candidate 46,XX true hermaphrodite Q99.2 Primary diagnosis candidate Fragile X chromosome Q99.8 Primary diagnosis candidate Other specified chromosome abnormalities Q99.9 Primary diagnosis candidate Chromosomal abnormality, unspecified