ICD-10-CM/PCS MS-DRG v36.0 Definitions Manual
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Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 195 of 312
PDX Collection 1114 (continued)
Q937Deletions with other complex rearrangements
Q9381Velo-cardio-facial syndrome
Q9382Williams syndrome
Q9388Other microdeletions
Q9389Other deletions from the autosomes
Q939Deletion from autosomes, unspecified
Q950Balanced translocation and insertion in normal individual
Q951Chromosome inversion in normal individual
Q952Balanced autosomal rearrangement in abnormal individual
Q953Balanced sex/autosomal rearrangement in abnormal individual
Q955Individual with autosomal fragile site
Q958Other balanced rearrangements and structural markers
Q959Balanced rearrangement and structural marker, unspecified
Q960Karyotype 45, X
Q961Karyotype 46, X iso (Xq)
Q962Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Q963Mosaicism, 45, X/46, XX or XY
Q964Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
Q968Other variants of Turner's syndrome
Q969Turner's syndrome, unspecified
Q970Karyotype 47, XXX
Q971Female with more than three X chromosomes
Q972Mosaicism, lines with various numbers of X chromosomes
Q973Female with 46, XY karyotype
Q978Other specified sex chromosome abnormalities, female phenotype
Q979Sex chromosome abnormality, female phenotype, unspecified
Q980Klinefelter syndrome karyotype 47, XXY
Q981Klinefelter syndrome, male with more than two X chromosomes
Q983Other male with 46, XX karyotype
Q984Klinefelter syndrome, unspecified
Q985Karyotype 47, XYY
Q986Male with structurally abnormal sex chromosome
Q987Male with sex chromosome mosaicism
Q988Other specified sex chromosome abnormalities, male phenotype
Q989Sex chromosome abnormality, male phenotype, unspecified
Q990Chimera 46, XX/46, XY
Q99146, XX true hermaphrodite
Q998Other specified chromosome abnormalities
Q999Chromosomal abnormality, unspecified
 
PDX Collection 1115
Q900Trisomy 21, nonmosaicism (meiotic nondisjunction)
Q901Trisomy 21, mosaicism (mitotic nondisjunction)
Q902Trisomy 21, translocation
Q909Down syndrome, unspecified
Q910Trisomy 18, nonmosaicism (meiotic nondisjunction)
Q911Trisomy 18, mosaicism (mitotic nondisjunction)
Q912Trisomy 18, translocation
Q913Trisomy 18, unspecified
Q914Trisomy 13, nonmosaicism (meiotic nondisjunction)
Q915Trisomy 13, mosaicism (mitotic nondisjunction)
Q916Trisomy 13, translocation
Q917Trisomy 13, unspecified
Q920Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
Q921Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
Q922Partial trisomy
Q925Duplications with other complex rearrangements
Q9261Marker chromosomes in normal individual
Q9262Marker chromosomes in abnormal individual
Q927Triploidy and polyploidy
Q928Other specified trisomies and partial trisomies of autosomes
Q929Trisomy and partial trisomy of autosomes, unspecified
Q930Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
Q931Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
Q932Chromosome replaced with ring, dicentric or isochromosome
Q934Deletion of short arm of chromosome 5
Q9381Velo-cardio-facial syndrome
Q9388Other microdeletions
Q950Balanced translocation and insertion in normal individual
Q951Chromosome inversion in normal individual
Q952Balanced autosomal rearrangement in abnormal individual
Q953Balanced sex/autosomal rearrangement in abnormal individual
Q955Individual with autosomal fragile site
Q958Other balanced rearrangements and structural markers
Q959Balanced rearrangement and structural marker, unspecified
Q960Karyotype 45, X
Q961Karyotype 46, X iso (Xq)
Q962Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Q963Mosaicism, 45, X/46, XX or XY
Q964Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
Q968Other variants of Turner's syndrome
Q969Turner's syndrome, unspecified
Q970Karyotype 47, XXX
Q971Female with more than three X chromosomes
Q972Mosaicism, lines with various numbers of X chromosomes
Q973Female with 46, XY karyotype
Q978Other specified sex chromosome abnormalities, female phenotype
Q979Sex chromosome abnormality, female phenotype, unspecified
Q980Klinefelter syndrome karyotype 47, XXY
Q981Klinefelter syndrome, male with more than two X chromosomes
Q983Other male with 46, XX karyotype
Q984Klinefelter syndrome, unspecified
Q985Karyotype 47, XYY
Q986Male with structurally abnormal sex chromosome
Q987Male with sex chromosome mosaicism
Q988Other specified sex chromosome abnormalities, male phenotype
Q989Sex chromosome abnormality, male phenotype, unspecified
Q990Chimera 46, XX/46, XY
Q99146, XX true hermaphrodite
Q998Other specified chromosome abnormalities
Q999Chromosomal abnormality, unspecified
 
PDX Collection 1116
Q900Trisomy 21, nonmosaicism (meiotic nondisjunction)
Q901Trisomy 21, mosaicism (mitotic nondisjunction)
Q902Trisomy 21, translocation
Q909Down syndrome, unspecified
Q910Trisomy 18, nonmosaicism (meiotic nondisjunction)
Q911Trisomy 18, mosaicism (mitotic nondisjunction)
Q912Trisomy 18, translocation
Q913Trisomy 18, unspecified
Q914Trisomy 13, nonmosaicism (meiotic nondisjunction)
Q915Trisomy 13, mosaicism (mitotic nondisjunction)
Q916Trisomy 13, translocation
Q917Trisomy 13, unspecified
Q920Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
Q921Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
Q922Partial trisomy
Q925Duplications with other complex rearrangements
Q9261Marker chromosomes in normal individual
Q9262Marker chromosomes in abnormal individual
Q927Triploidy and polyploidy
Q928Other specified trisomies and partial trisomies of autosomes
Q929Trisomy and partial trisomy of autosomes, unspecified
Q930Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
Q931Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
Q932Chromosome replaced with ring, dicentric or isochromosome
Q933Deletion of short arm of chromosome 4
Q9351Angelman syndrome
Q9359Other deletions of part of a chromosome
Q937Deletions with other complex rearrangements
Q9381Velo-cardio-facial syndrome
Q9382Williams syndrome
Q9388Other microdeletions
Q9389Other deletions from the autosomes
Q939Deletion from autosomes, unspecified
Q950Balanced translocation and insertion in normal individual
Q951Chromosome inversion in normal individual
Q952Balanced autosomal rearrangement in abnormal individual
Q953Balanced sex/autosomal rearrangement in abnormal individual
Q955Individual with autosomal fragile site
Q958Other balanced rearrangements and structural markers
Q959Balanced rearrangement and structural marker, unspecified
Q960Karyotype 45, X
Q961Karyotype 46, X iso (Xq)
Q962Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Q963Mosaicism, 45, X/46, XX or XY
Q964Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
Q968Other variants of Turner's syndrome
Q969Turner's syndrome, unspecified
Q970Karyotype 47, XXX
Q971Female with more than three X chromosomes
Q972Mosaicism, lines with various numbers of X chromosomes
Q973Female with 46, XY karyotype
Q978Other specified sex chromosome abnormalities, female phenotype
Q979Sex chromosome abnormality, female phenotype, unspecified
Q980Klinefelter syndrome karyotype 47, XXY
Q981Klinefelter syndrome, male with more than two X chromosomes
Q983Other male with 46, XX karyotype
Q984Klinefelter syndrome, unspecified
Q985Karyotype 47, XYY
Q986Male with structurally abnormal sex chromosome
Q987Male with sex chromosome mosaicism
Q988Other specified sex chromosome abnormalities, male phenotype
Q989Sex chromosome abnormality, male phenotype, unspecified
Q990Chimera 46, XX/46, XY
Q99146, XX true hermaphrodite
Q998Other specified chromosome abnormalities
Q999Chromosomal abnormality, unspecified
 
PDX Collection 1117
Q900Trisomy 21, nonmosaicism (meiotic nondisjunction)
Q901Trisomy 21, mosaicism (mitotic nondisjunction)
Q902Trisomy 21, translocation
Q909Down syndrome, unspecified
Q910Trisomy 18, nonmosaicism (meiotic nondisjunction)
Q911Trisomy 18, mosaicism (mitotic nondisjunction)
Q912Trisomy 18, translocation
Q913Trisomy 18, unspecified
Q914Trisomy 13, nonmosaicism (meiotic nondisjunction)
Q915Trisomy 13, mosaicism (mitotic nondisjunction)
Q916Trisomy 13, translocation
Q917Trisomy 13, unspecified
Q920Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
Q921Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
Q922Partial trisomy
Q925Duplications with other complex rearrangements
Q9261Marker chromosomes in normal individual
Q9262Marker chromosomes in abnormal individual
Q927Triploidy and polyploidy
Q928Other specified trisomies and partial trisomies of autosomes
Q929Trisomy and partial trisomy of autosomes, unspecified
Q930Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
Q931Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
Q932Chromosome replaced with ring, dicentric or isochromosome
Q933Deletion of short arm of chromosome 4
Q934Deletion of short arm of chromosome 5
Q9351Angelman syndrome
Q9359Other deletions of part of a chromosome
Q937Deletions with other complex rearrangements
Q9382Williams syndrome
Q9388Other microdeletions
Q9389Other deletions from the autosomes
Q939Deletion from autosomes, unspecified
Q950Balanced translocation and insertion in normal individual
Q951Chromosome inversion in normal individual
Q952Balanced autosomal rearrangement in abnormal individual
Q953Balanced sex/autosomal rearrangement in abnormal individual
Q955Individual with autosomal fragile site
Q958Other balanced rearrangements and structural markers
Q959Balanced rearrangement and structural marker, unspecified
Q960Karyotype 45, X
Q961Karyotype 46, X iso (Xq)
Q962Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Q963Mosaicism, 45, X/46, XX or XY
Q964Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
Q968Other variants of Turner's syndrome
Q969Turner's syndrome, unspecified
Q970Karyotype 47, XXX
Q971Female with more than three X chromosomes
Q972Mosaicism, lines with various numbers of X chromosomes
Q973Female with 46, XY karyotype
Q978Other specified sex chromosome abnormalities, female phenotype
Q979Sex chromosome abnormality, female phenotype, unspecified
Q980Klinefelter syndrome karyotype 47, XXY
Q981Klinefelter syndrome, male with more than two X chromosomes
Q983Other male with 46, XX karyotype
Q984Klinefelter syndrome, unspecified
Q985Karyotype 47, XYY
Q986Male with structurally abnormal sex chromosome
Q987Male with sex chromosome mosaicism
Q988Other specified sex chromosome abnormalities, male phenotype
Q989Sex chromosome abnormality, male phenotype, unspecified
Q990Chimera 46, XX/46, XY
Q99146, XX true hermaphrodite
Q998Other specified chromosome abnormalities
Q999Chromosomal abnormality, unspecified
 
PDX Collection 1118
Q900Trisomy 21, nonmosaicism (meiotic nondisjunction)
Q901Trisomy 21, mosaicism (mitotic nondisjunction)
Q902Trisomy 21, translocation
Q909Down syndrome, unspecified
Q910Trisomy 18, nonmosaicism (meiotic nondisjunction)
Q911Trisomy 18, mosaicism (mitotic nondisjunction)
Q912Trisomy 18, translocation
Q913Trisomy 18, unspecified
Q914Trisomy 13, nonmosaicism (meiotic nondisjunction)
Q915Trisomy 13, mosaicism (mitotic nondisjunction)
Q916Trisomy 13, translocation
Q917Trisomy 13, unspecified
Q920Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
Q921Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
Q922Partial trisomy
Q925Duplications with other complex rearrangements
Q9261Marker chromosomes in normal individual
Q9262Marker chromosomes in abnormal individual
Q927Triploidy and polyploidy
Q928Other specified trisomies and partial trisomies of autosomes
Q929Trisomy and partial trisomy of autosomes, unspecified
Q930Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
Q931Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
Q932Chromosome replaced with ring, dicentric or isochromosome
Q933Deletion of short arm of chromosome 4
Q934Deletion of short arm of chromosome 5
Q9351Angelman syndrome
Q9359Other deletions of part of a chromosome
Q937Deletions with other complex rearrangements
Q9381Velo-cardio-facial syndrome
Q9382Williams syndrome
Q9389Other deletions from the autosomes
Q939Deletion from autosomes, unspecified
Q950Balanced translocation and insertion in normal individual
Q951Chromosome inversion in normal individual
Q952Balanced autosomal rearrangement in abnormal individual
Q953Balanced sex/autosomal rearrangement in abnormal individual
Q955Individual with autosomal fragile site
Q958Other balanced rearrangements and structural markers
Q959Balanced rearrangement and structural marker, unspecified
Q960Karyotype 45, X
Q961Karyotype 46, X iso (Xq)
Q962Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Q963Mosaicism, 45, X/46, XX or XY
Q964Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
Q968Other variants of Turner's syndrome
Q969Turner's syndrome, unspecified
Q970Karyotype 47, XXX
Q971Female with more than three X chromosomes
Q972Mosaicism, lines with various numbers of X chromosomes
Q973Female with 46, XY karyotype
Q978Other specified sex chromosome abnormalities, female phenotype
Q979Sex chromosome abnormality, female phenotype, unspecified
Q980Klinefelter syndrome karyotype 47, XXY
Q981Klinefelter syndrome, male with more than two X chromosomes
Q983Other male with 46, XX karyotype
Q984Klinefelter syndrome, unspecified
Q985Karyotype 47, XYY
Q986Male with structurally abnormal sex chromosome
Q987Male with sex chromosome mosaicism
Q988Other specified sex chromosome abnormalities, male phenotype
Q989Sex chromosome abnormality, male phenotype, unspecified
Q990Chimera 46, XX/46, XY
Q99146, XX true hermaphrodite
Q998Other specified chromosome abnormalities
Q999Chromosomal abnormality, unspecified
 
PDX Collection 1119
R042Hemoptysis
R0481Acute idiopathic pulmonary hemorrhage in infants
R0489Hemorrhage from other sites in respiratory passages
R049Hemorrhage from respiratory passages, unspecified
R093Abnormal sputum
R6813Apparent life threatening event in infant (ALTE)
 
PDX Collection 1120
J22Unspecified acute lower respiratory infection
J80Acute respiratory distress syndrome
J9600Acute respiratory failure, unspecified whether with hypoxia or hypercapnia
J9601Acute respiratory failure with hypoxia
J9602Acute respiratory failure with hypercapnia
J9610Chronic respiratory failure, unspecified whether with hypoxia or hypercapnia
J9611Chronic respiratory failure with hypoxia
J9612Chronic respiratory failure with hypercapnia
J9620Acute and chronic respiratory failure, unspecified whether with hypoxia or hypercapnia
J9621Acute and chronic respiratory failure with hypoxia
J9622Acute and chronic respiratory failure with hypercapnia
J9690Respiratory failure, unspecified, unspecified whether with hypoxia or hypercapnia
J9691Respiratory failure, unspecified with hypoxia
J9692Respiratory failure, unspecified with hypercapnia
J988Other specified respiratory disorders
J989Respiratory disorder, unspecified
R063Periodic breathing
R0681Apnea, not elsewhere classified
R092Respiratory arrest
 
PDX Collection 1121
G890Central pain syndrome
G8911Acute pain due to trauma
G8912Acute post-thoracotomy pain
G8918Other acute postprocedural pain
G8921Chronic pain due to trauma
G8922Chronic post-thoracotomy pain
G8928Other chronic postprocedural pain
G8929Other chronic pain
G893Neoplasm related pain (acute) (chronic)
G894Chronic pain syndrome
J80Acute respiratory distress syndrome
J9600Acute respiratory failure, unspecified whether with hypoxia or hypercapnia
J9601Acute respiratory failure with hypoxia
J9602Acute respiratory failure with hypercapnia
J9610Chronic respiratory failure, unspecified whether with hypoxia or hypercapnia
J9611Chronic respiratory failure with hypoxia
J9612Chronic respiratory failure with hypercapnia
J9620Acute and chronic respiratory failure, unspecified whether with hypoxia or hypercapnia
J9621Acute and chronic respiratory failure with hypoxia
J9622Acute and chronic respiratory failure with hypercapnia
J9690Respiratory failure, unspecified, unspecified whether with hypoxia or hypercapnia
J9691Respiratory failure, unspecified with hypoxia
J9692Respiratory failure, unspecified with hypercapnia
R0901Asphyxia
R0902Hypoxemia
R092Respiratory arrest
R29700NIHSS score 0
R29701NIHSS score 1
R29702NIHSS score 2
R29703NIHSS score 3
R29704NIHSS score 4
R29705NIHSS score 5
R29706NIHSS score 6
R29707NIHSS score 7
R29708NIHSS score 8
R29709NIHSS score 9
R29710NIHSS score 10
R29711NIHSS score 11
R29712NIHSS score 12
R29713NIHSS score 13
R29714NIHSS score 14
R29715NIHSS score 15
R29716NIHSS score 16
R29717NIHSS score 17
R29718NIHSS score 18
R29719NIHSS score 19
R29720NIHSS score 20
R29721NIHSS score 21
R29722NIHSS score 22
R29723NIHSS score 23
R29724NIHSS score 24
R29725NIHSS score 25
R29726NIHSS score 26
R29727NIHSS score 27
R29728NIHSS score 28
R29729NIHSS score 29
R29730NIHSS score 30
R29731NIHSS score 31
R29732NIHSS score 32
R29733NIHSS score 33
R29734NIHSS score 34
R29735NIHSS score 35
R29736NIHSS score 36
R29737NIHSS score 37
R29738NIHSS score 38
R29739NIHSS score 39
R29740NIHSS score 40
R29741NIHSS score 41
R29742NIHSS score 42
R410Disorientation, unspecified
R411Anterograde amnesia
R412Retrograde amnesia
R413Other amnesia
R4182Altered mental status, unspecified
R419Unspecified symptoms and signs involving cognitive functions and awareness
R448Other symptoms and signs involving general sensations and perceptions
R449Unspecified symptoms and signs involving general sensations and perceptions
R4583Excessive crying of child, adolescent or adult
R4584Anhedonia



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