Certain infectious and parasitic diseases
Certain infectious and parasitic diseases Certain infectious and parasitic diseases
Q93 Monosomies and deletions from the autosomes, not elsewhere classified Q93.0 Whole chromosome monosomy, meiotic nondisjunction Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction) Q93.2 Chromosome replaced with ring or dicentric Q93.3 Deletion of short arm of chromosome 4 Wolff-Hirschorn syndrome Q93.4 Deletion of short arm of chromosome 5 Cri-du-chat syndrome Q93.5 Other deletions of part of a chromosome Angelman syndrome Q93.6 Deletions seen only at prometaphase Q93.7 Deletions with other complex rearrangements Q93.8 Other deletions from the autosomes Q93.9 Deletion from autosomes, unspecified Q95 Balanced rearrangements and structural markers, not elsewhere classified Includes: Robertsonian and balanced reciprocal translocations and insertions Q95.0 Balanced translocation and insertion in normal individual Q95.1 Chromosome inversion in normal individual Q95.2 Balanced autosomal rearrangement in abnormal individual Q95.3 Balanced sex/autosomal rearrangement in abnormal individual Q95.4 Individuals with marker heterochromatin Q95.5 Individuals with autosomal fragile site Q95.8 Other balanced rearrangements and structural markers Q95.9 Balanced rearrangement and structural marker, unspecified Q96 Turner's syndrome Excludes: Noonan's syndrome ( Q87.1 ) Q96.0 Karyotype 45,X Q96.1 Karyotype 46,X iso (Xq) Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq) Q96.3 Mosaicism, 45,X/46,XX or XY Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome 582 WHO’s ICD-10
Q96.8 Other variants of Turner's syndrome Q96.9 Turner's syndrome, unspecified Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified Excludes: Turner's syndrome ( Q96.- ) Q97.0 Karyotype 47,XXX Q97.1 Female with more than three X chromosomes Q97.2 Mosaicism, lines with various numbers of X chromosomes Q97.3 Female with 46,XY karyotype Q97.8 Other specified sex chromosome abnormalities, female phenotype Q97.9 Sex chromosome abnormality, female phenotype, unspecified Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified Q98.0 Klinefelter's syndrome karyotype 47,XXY Q98.1 Klinefelter's syndrome, male with more than two X chromosomes Q98.2 Klinefelter's syndrome, male with 46,XX karyotype Q98.3 Other male with 46,XX karyotype Q98.4 Klinefelter's syndrome, unspecified Q98.5 Karyotype 47,XYY Q98.6 Male with structurally abnormal sex chromosome Q98.7 Male with sex chromosome mosaicism Q98.8 Other specified sex chromosome abnormalities, male phenotype Q98.9 Sex chromosome abnormality, male phenotype, unspecified Q99 Other chromosome abnormalities, not elsewhere classified Q99.0 Chimera 46,XX/46,XY Chimera 46,XX/46,XY true hermaphrodite Q99.1 46,XX true hermaphrodite 46,XX with streak gonads 46,XY with streak gonads Pure gonadal dysgenesis Q99.2 Fragile X chromosome Fragile X syndrome Q99.8 Other specified chromosome abnormalities Q99.9 Chromosomal abnormality, unspecified Version for 2007 583
- Page 531 and 532: P61.5 Transient neonatal neutropeni
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- Page 535 and 536: P92 Feeding problems of newborn P92
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- Page 539 and 540: Agyria Hydranencephaly Lissencephal
- Page 541 and 542: Congenital malformations of eye, ea
- Page 543 and 544: Q14 Congenital malformations of pos
- Page 545 and 546: Q18.1 Preauricular sinus and cyst F
- Page 547 and 548: Q22.2 Congenital pulmonary valve in
- Page 549 and 550: Double aortic arch [vascular ring o
- Page 551 and 552: Q28.1 Other malformations of precer
- Page 553 and 554: Q33.2 Sequestration of lung Q33.3 A
- Page 555 and 556: Q38.1 Ankyloglossia Tongue tie Q38.
- Page 557 and 558: Q41.1 Congenital absence, atresia a
- Page 559 and 560: Q44.7 Other congenital malformation
- Page 561 and 562: Q51.6 Embryonic cyst of cervix Q51.
- Page 563 and 564: Q56 Indeterminate sex and pseudoher
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- Page 567 and 568: Q66.2 Metatarsus varus Q66.3 Other
- Page 569 and 570: Q69.2 Accessory toe(s) Accessory ha
- Page 571 and 572: Q74.1 Congenital malformation of kn
- Page 573 and 574: Q76.6 Other congenital malformation
- Page 575 and 576: Q79.8 Other congenital malformation
- Page 577 and 578: Q83 Congenital malformations of bre
- Page 579 and 580: Q87 Other specified congenital malf
- Page 581: Chromosomal abnormalities, not else
- Page 585 and 586: R70-R79 Abnormal findings on examin
- Page 587 and 588: R06.0 Dyspnoea Orthopnoea Shortness
- Page 589 and 590: Symptoms and signs involving the di
- Page 591 and 592: . R19.2 Visible peristalsis Hyperpe
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- Page 595 and 596: R31 R32 R33 R34 R35 R36 Unspecified
- Page 597 and 598: R42 Dizziness and giddiness Light-h
- Page 599 and 600: R49.1 Aphonia Loss of voice R49.2 H
- Page 601 and 602: R55 Syncope and collapse Blackout F
- Page 603 and 604: R61 Hyperhidrosis R61.0 Localized h
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- Page 607 and 608: R78.0 Finding of alcohol in blood U
- Page 609 and 610: R82.7 Abnormal findings on microbio
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- Page 613 and 614: R94.8 Abnormal results of function
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- Page 623 and 624: S08 Traumatic amputation of part of
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- Page 629 and 630: S24 Injury of nerves and spinal cor
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Q96.8 Other variants of Turner's syndrome<br />
Q96.9 Turner's syndrome, unspecified<br />
Q97 Other sex chromosome abnormalities, female phenotype,<br />
not elsewhere classified<br />
Excludes: Turner's syndrome ( Q96.- )<br />
Q97.0 Karyotype 47,XXX<br />
Q97.1 Female with more than three X chromosomes<br />
Q97.2 Mosaicism, lines with various numbers of X chromosomes<br />
Q97.3 Female with 46,XY karyotype<br />
Q97.8 Other specified sex chromosome abnormalities, female phenotype<br />
Q97.9 Sex chromosome abnormality, female phenotype, unspecified<br />
Q98<br />
Other sex chromosome abnormalities, male phenotype,<br />
not elsewhere classified<br />
Q98.0 Klinefelter's syndrome karyotype 47,XXY<br />
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes<br />
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype<br />
Q98.3 Other male with 46,XX karyotype<br />
Q98.4 Klinefelter's syndrome, unspecified<br />
Q98.5 Karyotype 47,XYY<br />
Q98.6 Male with structurally abnormal sex chromosome<br />
Q98.7 Male with sex chromosome mosaicism<br />
Q98.8 Other specified sex chromosome abnormalities, male phenotype<br />
Q98.9 Sex chromosome abnormality, male phenotype, unspecified<br />
Q99<br />
Other chromosome abnormalities, not elsewhere classified<br />
Q99.0 Chimera 46,XX/46,XY<br />
Chimera 46,XX/46,XY true hermaphrodite<br />
Q99.1 46,XX true hermaphrodite<br />
46,XX with streak gonads<br />
46,XY with streak gonads<br />
Pure gonadal dysgenesis<br />
Q99.2 Fragile X chromosome<br />
Fragile X syndrome<br />
Q99.8 Other specified chromosome abnormalities<br />
Q99.9 Chromosomal abnormality, unspecified<br />
Version for 2007 583
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