 Q92 |
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Other trisomies and partial trisomies of the autosomes, not elsewhere classified  |
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| Includes |
unbalanced translocations and insertions
|
| Excludes1 |
trisomies of chromosomes 13, 18, 21 (Q90-Q91)
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|
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 Q92.0 |
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Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction) |
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| |
| Q92.1 |
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Whole chromosome trisomy, mosaicism (mitotic nondisjunction) |
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| Q92.2 |
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Partial trisomy |
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| Less than whole arm duplicated | | Whole arm or more duplicated |
| Excludes1 |
partial trisomy due to unbalanced translocation (Q92.5)
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|
|
| |
| Q92.5 |
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Duplications with other complex rearrangements |
| |
| Partial trisomy due to unbalanced translocations |
| CodeAlso |
any associated deletions due to unbalanced translocations, inversions and insertions (Q93.7)
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|
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| Q92.6 |
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Marker chromosomes |
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| Trisomies due to dicentrics | | Trisomies due to extra rings | | Trisomies due to isochromosomes | | Individual with marker heterochromatin |
|
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| Q92.61 |
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Marker chromosomes in normal individual |
| | |
| Q92.62 |
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Marker chromosomes in abnormal individual |
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| Q92.7 |
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Triploidy and polyploidy |
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| Q92.8 |
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Other specified trisomies and partial trisomies of autosomes |
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| Duplications identified by fluorescence in situ hybridization (FISH) | | Duplications identified by in situ hybridization (ISH) | | Duplications seen only at prometaphase |
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| Q92.9 |
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Trisomy and partial trisomy of autosomes, unspecified |
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