 Q93 |
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Monosomies and deletions from the autosomes, not elsewhere classified  |
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 Q93.0 |
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Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction) |
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| Q93.1 |
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Whole chromosome monosomy, mosaicism (mitotic nondisjunction) |
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| Q93.2 |
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Chromosome replaced with ring, dicentric or isochromosome |
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| Q93.3 |
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Deletion of short arm of chromosome 4 |
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| Q93.4 |
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Deletion of short arm of chromosome 5 |
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| Q93.5 |
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Other deletions of part of a chromosome |
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| Q93.51 |
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Angelman syndrome |
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| Q93.52 |
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Phelan-McDermid syndrome |
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| 22q13.3 deletion syndrome |
| UseAdditionalCode |
code(s) to identify any associated conditions, such as:
autism spectrum disorder (F84.0)
degree of intellectual disabilities (F70-F79)
epilepsy and recurrent seizures (G40.-)
lymphedema (I89.0)
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| Q93.59 |
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Other deletions of part of a chromosome |
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| Q93.7 |
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Deletions with other complex rearrangements |
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| Deletions due to unbalanced translocations, inversions and insertions |
| CodeAlso |
any associated duplications due to unbalanced translocations, inversions and insertions (Q92.5)
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| Q93.8 |
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Other deletions from the autosomes |
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| Q93.81 |
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Velo-cardio-facial syndrome |
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| Q93.82 |
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Williams syndrome |
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| Q93.88 |
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Other microdeletions |
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| Miller-Dieker syndrome | | Smith-Magenis syndrome |
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| Q93.89 |
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Other deletions from the autosomes |
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| Deletions identified by fluorescence in situ hybridization (FISH) | | Deletions identified by in situ hybridization (ISH) | | Deletions seen only at prometaphase |
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| Q93.9 |
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Deletion from autosomes, unspecified |
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