ICD-10-CM/PCS MS-DRG v35.0 Definitions Manual
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Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 197 of 313
 
PDX Collection 1104
Q773Chondrodysplasia punctata
Q776Chondroectodermal dysplasia
Q780Osteogenesis imperfecta
Q781Polyostotic fibrous dysplasia
Q782Osteopetrosis
Q783Progressive diaphyseal dysplasia
Q785Metaphyseal dysplasia
Q786Multiple congenital exostoses
Q788Other specified osteochondrodysplasias
Q789Osteochondrodysplasia, unspecified
 
PDX Collection 1105
Q401Congenital hiatus hernia
Q790Congenital diaphragmatic hernia
Q791Other congenital malformations of diaphragm
 
PDX Collection 1106
Q792Exomphalos
Q793Gastroschisis
Q794Prune belly syndrome
Q7951Congenital hernia of bladder
Q7959Other congenital malformations of abdominal wall
 
PDX Collection 1107
Q796Ehlers-Danlos syndrome
 
PDX Collection 1108
Q851Tuberous sclerosis
Q858Other phakomatoses, not elsewhere classified
Q859Phakomatosis, unspecified
Q897Multiple congenital malformations, not elsewhere classified
Q899Congenital malformation, unspecified
 
PDX Collection 1109
Q858Other phakomatoses, not elsewhere classified
Q859Phakomatosis, unspecified
Q899Congenital malformation, unspecified
 
PDX Collection 1110
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
Q858Other phakomatoses, not elsewhere classified
Q859Phakomatosis, unspecified
Q871Congenital malformation syndromes predominantly associated with short stature
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q8740Marfan's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations
Q8743Marfan's syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q899Congenital malformation, unspecified
Q992Fragile X chromosome
 
PDX Collection 1111
Q8901Asplenia (congenital)
Q8909Congenital malformations of spleen
Q899Congenital malformation, unspecified
 
PDX Collection 1112
Q893Situs inversus
Q897Multiple congenital malformations, not elsewhere classified
Q899Congenital malformation, unspecified
 
PDX Collection 1113
Q894Conjoined twins
Q897Multiple congenital malformations, not elsewhere classified
Q899Congenital malformation, unspecified
 
PDX Collection 1114
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
Q935Other deletions of part of a chromosome
Q937Deletions with other complex rearrangements
Q9381Velo-cardio-facial 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
Q935Other deletions of part of a chromosome
Q937Deletions with other complex rearrangements
Q9381Velo-cardio-facial 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
Q935Other deletions of part of a chromosome
Q937Deletions with other complex rearrangements
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
Q935Other deletions of part of a chromosome
Q937Deletions with other complex rearrangements
Q9381Velo-cardio-facial 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



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