Source |
Code |
Name |
Case count |
Share of cases (%) |
OUTPAT |
OUTPAT_ICD10(Q998) |
Other specified chromosome abnormalities |
79 |
|
OUTPAT |
OUTPAT_ICD10(Q950) |
Balanced translocation and insertion in normal individual |
74 |
|
OUTPAT |
OUTPAT_ICD10(Q909) |
Down's syndrome, unspecified |
65 |
|
OUTPAT |
OUTPAT_ICD10(Q900) |
Trisomy 21, meiotic nondisjunction |
54 |
|
INPAT |
INPAT_ICD10(Q909) |
Down's syndrome, unspecified |
48 |
|
INPAT |
INPAT_ICD10(Q900) |
Trisomy 21, meiotic nondisjunction |
41 |
|
OUTPAT |
OUTPAT_ICD10(Q938) |
Other deletions from the autosomes |
34 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(Q90) |
Down's syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
28 |
|
INPAT |
INPAT_ICD10(Q998) |
Other specified chromosome abnormalities |
25 |
|
OUTPAT |
OUTPAT_ICD10(Q935) |
Other deletions of part of a chromosome |
25 |
|
OUTPAT |
OUTPAT_ICD10(Q992) |
Fragile X chromosome |
22 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(Q909) |
Down's syndrome, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
22 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(Q998) |
Other specified chromosome abnormalities. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
19 |
|
OUTPAT |
OUTPAT_ICD10(Q980) |
Klinefelter's syndrome karyotype 47,XXY |
16 |
|
OUTPAT |
OUTPAT_ICD10(Q985) |
Karyotype 47,XYY |
15 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(Q900) |
Trisomy 21, meiotic nondisjunction. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
14 |
|
OUTPAT |
OUTPAT_ICD10(Q988) |
Other specified sex chromosome abnormalities, male phenotype |
12 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(Q938) |
Other deletions from the autosomes. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
12 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(Q992) |
Fragile X chromosome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
12 |
|
INPAT |
INPAT_ICD10(Q935) |
Other deletions of part of a chromosome |
11 |
|
OUTPAT |
OUTPAT_ICD10(Q951) |
Chromosome inversion in normal individual |
11 |
|
OUTPAT |
OUTPAT_ICD10(Q963) |
Mosaicism, 45,X/46,XX or XY |
11 |
|
INPAT |
INPAT_ICD10(Q938) |
Other deletions from the autosomes |
10 |
|
OUTPAT |
OUTPAT_ICD10(Q958) |
Other balanced rearrangements and structural markers |
10 |
|
OUTPAT |
OUTPAT_ICD10(Q968) |
Other variants of Turner's syndrome |
10 |
|
OUTPAT |
OUTPAT_ICD10(Q970) |
Karyotype 47,XXX |
10 |
|
DEATH |
DEATH_ICD10(Q909) |
Down's syndrome, unspecified |
9 |
|
OUTPAT |
OUTPAT_ICD10(Q901) |
Trisomy 21, mosaicism (mitotic nondisjunction) |
9 |
|
INPAT |
INPAT_ICD10(Q980) |
Klinefelter's syndrome karyotype 47,XXY |
8 |
|
INPAT |
INPAT_ICD10(Q992) |
Fragile X chromosome |
8 |
|
OUTPAT |
OUTPAT_ICD10(Q90) |
Down's syndrome |
8 |
|
OUTPAT |
OUTPAT_ICD10(Q910) |
Trisomy 18, meiotic nondisjunction |
8 |
|
OUTPAT |
OUTPAT_ICD10(Q923) |
Minor partial trisomy |
8 |
|
OUTPAT |
OUTPAT_ICD10(Q928) |
Other specified trisomies and partial trisomies of autosomes |
8 |
|
OUTPAT |
OUTPAT_ICD10(Q952) |
Balanced autosomal rearrangement in abnormal individual |
8 |
|
OUTPAT |
OUTPAT_ICD10(Q984) |
Klinefelter's syndrome, unspecified |
8 |
|
OUTPAT |
OUTPAT_ICD10(Q999) |
Chromosomal abnormality, unspecified |
8 |
|
INPAT |
INPAT_ICD10(Q950) |
Balanced translocation and insertion in normal individual |
7 |
|
OUTPAT |
OUTPAT_ICD10(Q960) |
Karyotype 45,X |
7 |
|
OUTPAT |
OUTPAT_ICD10(Q972) |
Mosaicism, lines with various numbers of X chromosomes |
7 |
|
OUTPAT |
OUTPAT_ICD10(Q986) |
Male with structurally abnormal sex chromosome |
7 |
|
INPAT |
INPAT_ICD10(Q970) |
Karyotype 47,XXX |
6 |
|
INPAT |
INPAT_ICD10(Q985) |
Karyotype 47,XYY |
6 |
|
OUTPAT |
OUTPAT_ICD10(Q902) |
Trisomy 21, translocation |
6 |
|
OUTPAT |
OUTPAT_ICD10(Q911) |
Trisomy 18, mosaicism (mitotic nondisjunction) |
6 |
|
OUTPAT |
OUTPAT_ICD10(Q930) |
Whole chromosome monosomy, meiotic nondisjunction |
6 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(Q984) |
Klinefelter's syndrome, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
6 |
|
INPAT |
INPAT_ICD10(Q913) |
Edwards syndrome, unspecified |
5 |
|
OUTPAT |
OUTPAT_ICD10(Q925) |
Duplications with other complex rearrangements |
5 |
|
OUTPAT |
OUTPAT_ICD10(Q978) |
Other specified sex chromosome abnormalities, female phenotype |
5 |
|
OUTPAT |
OUTPAT_ICD10(Q991) |
46,XX true hermaphrodite |
5 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(Q935) |
Other deletions of part of a chromosome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
5 |
|