| PDX Collection 1544 (continued) |
| Q958 | Other balanced rearrangements and structural markers |
| Q959 | Balanced rearrangement and structural marker, unspecified |
| Q960 | Karyotype 45, X |
| Q961 | Karyotype 46, X iso (Xq) |
| Q962 | Karyotype 46, X with abnormal sex chromosome, except iso (Xq) |
| Q963 | Mosaicism, 45, X/46, XX or XY |
| Q964 | Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome |
| Q968 | Other variants of Turner's syndrome |
| Q969 | Turner's syndrome, unspecified |
| Q970 | Karyotype 47, XXX |
| Q971 | Female with more than three X chromosomes |
| Q972 | Mosaicism, lines with various numbers of X chromosomes |
| Q973 | Female with 46, XY karyotype |
| Q978 | Other specified sex chromosome abnormalities, female phenotype |
| Q979 | Sex chromosome abnormality, female phenotype, unspecified |
| Q980 | Klinefelter syndrome karyotype 47, XXY |
| Q981 | Klinefelter syndrome, male with more than two X chromosomes |
| Q983 | Other male with 46, XX karyotype |
| Q984 | Klinefelter syndrome, unspecified |
| Q985 | Karyotype 47, XYY |
| Q986 | Male with structurally abnormal sex chromosome |
| Q987 | Male with sex chromosome mosaicism |
| Q988 | Other specified sex chromosome abnormalities, male phenotype |
| Q989 | Sex chromosome abnormality, male phenotype, unspecified |
| Q990 | Chimera 46, XX/46, XY |
| Q991 | 46, XX true hermaphrodite |
| Q9989 | Other specified chromosome abnormalities |
| Q999 | Chromosomal abnormality, unspecified |
| |
| PDX Collection 1545 |
| Q900 | Trisomy 21, nonmosaicism (meiotic nondisjunction) |
| Q901 | Trisomy 21, mosaicism (mitotic nondisjunction) |
| Q902 | Trisomy 21, translocation |
| Q909 | Down syndrome, unspecified |
| Q910 | Trisomy 18, nonmosaicism (meiotic nondisjunction) |
| Q911 | Trisomy 18, mosaicism (mitotic nondisjunction) |
| Q912 | Trisomy 18, translocation |
| Q913 | Trisomy 18, unspecified |
| Q914 | Trisomy 13, nonmosaicism (meiotic nondisjunction) |
| Q915 | Trisomy 13, mosaicism (mitotic nondisjunction) |
| Q916 | Trisomy 13, translocation |
| Q917 | Trisomy 13, unspecified |
| Q920 | Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction) |
| Q921 | Whole chromosome trisomy, mosaicism (mitotic nondisjunction) |
| Q922 | Partial trisomy |
| Q925 | Duplications with other complex rearrangements |
| Q9261 | Marker chromosomes in normal individual |
| Q9262 | Marker chromosomes in abnormal individual |
| Q927 | Triploidy and polyploidy |
| Q928 | Other specified trisomies and partial trisomies of autosomes |
| Q929 | Trisomy and partial trisomy of autosomes, unspecified |
| Q930 | Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction) |
| Q931 | Whole chromosome monosomy, mosaicism (mitotic nondisjunction) |
| Q932 | Chromosome replaced with ring, dicentric or isochromosome |
| Q934 | Deletion of short arm of chromosome 5 |
| Q937 | Deletions with other complex rearrangements |
| Q9381 | Velo-cardio-facial syndrome |
| Q9388 | Other microdeletions |
| Q950 | Balanced translocation and insertion in normal individual |
| Q951 | Chromosome inversion in normal individual |
| Q952 | Balanced autosomal rearrangement in abnormal individual |
| Q953 | Balanced sex/autosomal rearrangement in abnormal individual |
| Q955 | Individual with autosomal fragile site |
| Q958 | Other balanced rearrangements and structural markers |
| Q959 | Balanced rearrangement and structural marker, unspecified |
| Q960 | Karyotype 45, X |
| Q961 | Karyotype 46, X iso (Xq) |
| Q962 | Karyotype 46, X with abnormal sex chromosome, except iso (Xq) |
| Q963 | Mosaicism, 45, X/46, XX or XY |
| Q964 | Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome |
| Q968 | Other variants of Turner's syndrome |
| Q969 | Turner's syndrome, unspecified |
| Q970 | Karyotype 47, XXX |
| Q971 | Female with more than three X chromosomes |
| Q972 | Mosaicism, lines with various numbers of X chromosomes |
| Q973 | Female with 46, XY karyotype |
| Q978 | Other specified sex chromosome abnormalities, female phenotype |
| Q979 | Sex chromosome abnormality, female phenotype, unspecified |
| Q980 | Klinefelter syndrome karyotype 47, XXY |
| Q981 | Klinefelter syndrome, male with more than two X chromosomes |
| Q983 | Other male with 46, XX karyotype |
| Q984 | Klinefelter syndrome, unspecified |
| Q985 | Karyotype 47, XYY |
| Q986 | Male with structurally abnormal sex chromosome |
| Q987 | Male with sex chromosome mosaicism |
| Q988 | Other specified sex chromosome abnormalities, male phenotype |
| Q989 | Sex chromosome abnormality, male phenotype, unspecified |
| Q990 | Chimera 46, XX/46, XY |
| Q991 | 46, XX true hermaphrodite |
| Q9989 | Other specified chromosome abnormalities |
| Q999 | Chromosomal abnormality, unspecified |
| |
| PDX Collection 1546 |
| Q900 | Trisomy 21, nonmosaicism (meiotic nondisjunction) |
| Q901 | Trisomy 21, mosaicism (mitotic nondisjunction) |
| Q902 | Trisomy 21, translocation |
| Q909 | Down syndrome, unspecified |
| Q910 | Trisomy 18, nonmosaicism (meiotic nondisjunction) |
| Q911 | Trisomy 18, mosaicism (mitotic nondisjunction) |
| Q912 | Trisomy 18, translocation |
| Q913 | Trisomy 18, unspecified |
| Q914 | Trisomy 13, nonmosaicism (meiotic nondisjunction) |
| Q915 | Trisomy 13, mosaicism (mitotic nondisjunction) |
| Q916 | Trisomy 13, translocation |
| Q917 | Trisomy 13, unspecified |
| Q920 | Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction) |
| Q921 | Whole chromosome trisomy, mosaicism (mitotic nondisjunction) |
| Q922 | Partial trisomy |
| Q925 | Duplications with other complex rearrangements |
| Q9261 | Marker chromosomes in normal individual |
| Q9262 | Marker chromosomes in abnormal individual |
| Q927 | Triploidy and polyploidy |
| Q928 | Other specified trisomies and partial trisomies of autosomes |
| Q929 | Trisomy and partial trisomy of autosomes, unspecified |
| Q930 | Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction) |
| Q931 | Whole chromosome monosomy, mosaicism (mitotic nondisjunction) |
| Q932 | Chromosome replaced with ring, dicentric or isochromosome |
| Q934 | Deletion of short arm of chromosome 5 |
| Q9381 | Velo-cardio-facial syndrome |
| Q9388 | Other microdeletions |
| Q9389 | Other deletions from the autosomes |
| Q950 | Balanced translocation and insertion in normal individual |
| Q951 | Chromosome inversion in normal individual |
| Q952 | Balanced autosomal rearrangement in abnormal individual |
| Q953 | Balanced sex/autosomal rearrangement in abnormal individual |
| Q955 | Individual with autosomal fragile site |
| Q958 | Other balanced rearrangements and structural markers |
| Q959 | Balanced rearrangement and structural marker, unspecified |
| Q960 | Karyotype 45, X |
| Q961 | Karyotype 46, X iso (Xq) |
| Q962 | Karyotype 46, X with abnormal sex chromosome, except iso (Xq) |
| Q963 | Mosaicism, 45, X/46, XX or XY |
| Q964 | Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome |
| Q968 | Other variants of Turner's syndrome |
| Q969 | Turner's syndrome, unspecified |
| Q970 | Karyotype 47, XXX |
| Q971 | Female with more than three X chromosomes |
| Q972 | Mosaicism, lines with various numbers of X chromosomes |
| Q973 | Female with 46, XY karyotype |
| Q978 | Other specified sex chromosome abnormalities, female phenotype |
| Q979 | Sex chromosome abnormality, female phenotype, unspecified |
| Q980 | Klinefelter syndrome karyotype 47, XXY |
| Q981 | Klinefelter syndrome, male with more than two X chromosomes |
| Q983 | Other male with 46, XX karyotype |
| Q984 | Klinefelter syndrome, unspecified |
| Q985 | Karyotype 47, XYY |
| Q986 | Male with structurally abnormal sex chromosome |
| Q987 | Male with sex chromosome mosaicism |
| Q988 | Other specified sex chromosome abnormalities, male phenotype |
| Q989 | Sex chromosome abnormality, male phenotype, unspecified |
| Q990 | Chimera 46, XX/46, XY |
| Q991 | 46, XX true hermaphrodite |
| Q9989 | Other specified chromosome abnormalities |
| Q999 | Chromosomal abnormality, unspecified |
| |
| PDX Collection 1547 |
| Q900 | Trisomy 21, nonmosaicism (meiotic nondisjunction) |
| Q901 | Trisomy 21, mosaicism (mitotic nondisjunction) |
| Q902 | Trisomy 21, translocation |
| Q909 | Down syndrome, unspecified |
| Q910 | Trisomy 18, nonmosaicism (meiotic nondisjunction) |
| Q911 | Trisomy 18, mosaicism (mitotic nondisjunction) |
| Q912 | Trisomy 18, translocation |
| Q913 | Trisomy 18, unspecified |
| Q914 | Trisomy 13, nonmosaicism (meiotic nondisjunction) |
| Q915 | Trisomy 13, mosaicism (mitotic nondisjunction) |
| Q916 | Trisomy 13, translocation |
| Q917 | Trisomy 13, unspecified |
| Q920 | Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction) |
| Q921 | Whole chromosome trisomy, mosaicism (mitotic nondisjunction) |
| Q922 | Partial trisomy |
| Q925 | Duplications with other complex rearrangements |
| Q9261 | Marker chromosomes in normal individual |
| Q9262 | Marker chromosomes in abnormal individual |
| Q927 | Triploidy and polyploidy |
| Q928 | Other specified trisomies and partial trisomies of autosomes |
| Q929 | Trisomy and partial trisomy of autosomes, unspecified |
| Q930 | Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction) |
| Q931 | Whole chromosome monosomy, mosaicism (mitotic nondisjunction) |
| Q932 | Chromosome replaced with ring, dicentric or isochromosome |
| Q934 | Deletion of short arm of chromosome 5 |
| Q9381 | Velo-cardio-facial syndrome |
| Q9388 | Other microdeletions |
| Q939 | Deletion from autosomes, unspecified |
| Q950 | Balanced translocation and insertion in normal individual |
| Q951 | Chromosome inversion in normal individual |
| Q952 | Balanced autosomal rearrangement in abnormal individual |
| Q953 | Balanced sex/autosomal rearrangement in abnormal individual |
| Q955 | Individual with autosomal fragile site |
| Q958 | Other balanced rearrangements and structural markers |
| Q959 | Balanced rearrangement and structural marker, unspecified |
| Q960 | Karyotype 45, X |
| Q961 | Karyotype 46, X iso (Xq) |
| Q962 | Karyotype 46, X with abnormal sex chromosome, except iso (Xq) |
| Q963 | Mosaicism, 45, X/46, XX or XY |
| Q964 | Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome |
| Q968 | Other variants of Turner's syndrome |
| Q969 | Turner's syndrome, unspecified |
| Q970 | Karyotype 47, XXX |
| Q971 | Female with more than three X chromosomes |
| Q972 | Mosaicism, lines with various numbers of X chromosomes |
| Q973 | Female with 46, XY karyotype |
| Q978 | Other specified sex chromosome abnormalities, female phenotype |
| Q979 | Sex chromosome abnormality, female phenotype, unspecified |
| Q980 | Klinefelter syndrome karyotype 47, XXY |
| Q981 | Klinefelter syndrome, male with more than two X chromosomes |
| Q983 | Other male with 46, XX karyotype |
| Q984 | Klinefelter syndrome, unspecified |
| Q985 | Karyotype 47, XYY |
| Q986 | Male with structurally abnormal sex chromosome |
| Q987 | Male with sex chromosome mosaicism |
| Q988 | Other specified sex chromosome abnormalities, male phenotype |
| Q989 | Sex chromosome abnormality, male phenotype, unspecified |
| Q990 | Chimera 46, XX/46, XY |
| Q991 | 46, XX true hermaphrodite |
| Q9989 | Other specified chromosome abnormalities |
| Q999 | Chromosomal abnormality, unspecified |
| |
| PDX Collection 1548 |
| R042 | Hemoptysis |
| R0481 | Acute idiopathic pulmonary hemorrhage in infants |
| R0489 | Hemorrhage from other sites in respiratory passages |
| R049 | Hemorrhage from respiratory passages, unspecified |
| R093 | Abnormal sputum |
| R6813 | Apparent life threatening event in infant (ALTE) |
| |
| PDX Collection 1549 |
| J22 | Unspecified acute lower respiratory infection |
| J80 | Acute respiratory distress syndrome |
| J9600 | Acute respiratory failure, unspecified whether with hypoxia or hypercapnia |
| J9601 | Acute respiratory failure with hypoxia |
| J9602 | Acute respiratory failure with hypercapnia |
| J9610 | Chronic respiratory failure, unspecified whether with hypoxia or hypercapnia |
| J9611 | Chronic respiratory failure with hypoxia |
| J9612 | Chronic respiratory failure with hypercapnia |
| J9620 | Acute and chronic respiratory failure, unspecified whether with hypoxia or hypercapnia |
| J9621 | Acute and chronic respiratory failure with hypoxia |
| J9622 | Acute and chronic respiratory failure with hypercapnia |
| J9690 | Respiratory failure, unspecified, unspecified whether with hypoxia or hypercapnia |
| J9691 | Respiratory failure, unspecified with hypoxia |
| J9692 | Respiratory failure, unspecified with hypercapnia |
| J988 | Other specified respiratory disorders |
| J989 | Respiratory disorder, unspecified |
| N80B1 | Endometriosis of pleura |
| N80B2 | Endometriosis of lung |
| N80B31 | Superficial endometriosis of diaphragm |
| N80B32 | Deep endometriosis of diaphragm |
| N80B39 | Endometriosis of diaphragm, unspecified depth |
| R063 | Periodic breathing |
| R0681 | Apnea, not elsewhere classified |
| R092 | Respiratory arrest |
| |
| PDX Collection 1550 |
| G890 | Central pain syndrome |
| G8911 | Acute pain due to trauma |
| G8912 | Acute post-thoracotomy pain |
| G8918 | Other acute postprocedural pain |
| G8921 | Chronic pain due to trauma |
| G8922 | Chronic post-thoracotomy pain |
| G8928 | Other chronic postprocedural pain |
| G8929 | Other chronic pain |
| G893 | Neoplasm related pain (acute) (chronic) |
| G894 | Chronic pain syndrome |
| J80 | Acute respiratory distress syndrome |
| J9600 | Acute respiratory failure, unspecified whether with hypoxia or hypercapnia |
| J9601 | Acute respiratory failure with hypoxia |
| J9602 | Acute respiratory failure with hypercapnia |
| J9610 | Chronic respiratory failure, unspecified whether with hypoxia or hypercapnia |
| J9611 | Chronic respiratory failure with hypoxia |
| J9612 | Chronic respiratory failure with hypercapnia |
| J9620 | Acute and chronic respiratory failure, unspecified whether with hypoxia or hypercapnia |
| J9621 | Acute and chronic respiratory failure with hypoxia |
| J9622 | Acute and chronic respiratory failure with hypercapnia |
| J9690 | Respiratory failure, unspecified, unspecified whether with hypoxia or hypercapnia |
| J9691 | Respiratory failure, unspecified with hypoxia |
| J9692 | Respiratory failure, unspecified with hypercapnia |
| R0901 | Asphyxia |
| R0902 | Hypoxemia |
| R092 | Respiratory arrest |
| R410 | Disorientation, unspecified |
| R411 | Anterograde amnesia |
| R412 | Retrograde amnesia |
| R413 | Other amnesia |
| R4182 | Altered mental status, unspecified |
| R419 | Unspecified symptoms and signs involving cognitive functions and awareness |
| R448 | Other symptoms and signs involving general sensations and perceptions |
| R449 | Unspecified symptoms and signs involving general sensations and perceptions |
| R4583 | Excessive crying of child, adolescent or adult |
| R4584 | Anhedonia |
| R460 | Very low level of personal hygiene |
| R461 | Bizarre personal appearance |
| R462 | Strange and inexplicable behavior |
| R463 | Overactivity |
| R464 | Slowness and poor responsiveness |
| R465 | Suspiciousness and marked evasiveness |
| R466 | Undue concern and preoccupation with stressful events |
| R467 | Verbosity and circumstantial detail obscuring reason for contact |
| R52 | Pain, unspecified |
| R680 | Hypothermia, not associated with low environmental temperature |
| R6811 | Excessive crying of infant (baby) |
| R6812 | Fussy infant (baby) |
| R6813 | Apparent life threatening event in infant (ALTE) |
| R6819 | Other nonspecific symptoms peculiar to infancy |
| R6881 | Early satiety |
| R6882 | Decreased libido |
| R6883 | Chills (without fever) |
| R6889 | Other general symptoms and signs |
| R69 | Illness, unspecified |
| |
| PDX Collection 1551 |
| P578 | Other specified kernicterus |
| P579 | Kernicterus, unspecified |
| P580 | Neonatal jaundice due to bruising |
| P581 | Neonatal jaundice due to bleeding |
| P582 | Neonatal jaundice due to infection |
| P583 | Neonatal jaundice due to polycythemia |
| P5841 | Neonatal jaundice due to drugs or toxins transmitted from mother |
| P5842 | Neonatal jaundice due to drugs or toxins given to newborn |
| P585 | Neonatal jaundice due to swallowed maternal blood |
| P588 | Neonatal jaundice due to other specified excessive hemolysis |
| P589 | Neonatal jaundice due to excessive hemolysis, unspecified |
| P590 | Neonatal jaundice associated with preterm delivery |
| P591 | Inspissated bile syndrome |
| P5920 | Neonatal jaundice from unspecified hepatocellular damage |
| P5929 | Neonatal jaundice from other hepatocellular damage |
| P593 | Neonatal jaundice from breast milk inhibitor |
| P598 | Neonatal jaundice from other specified causes |
| P599 | Neonatal jaundice, unspecified |
| R17 | Unspecified jaundice |
| R238 | Other skin changes |
| R239 | Unspecified skin changes |
| |
| PDX Collection 1552 |
| G890 | Central pain syndrome |
| G8911 | Acute pain due to trauma |
| G8912 | Acute post-thoracotomy pain |
| G8918 | Other acute postprocedural pain |
| G8921 | Chronic pain due to trauma |
| G8922 | Chronic post-thoracotomy pain |
| G8928 | Other chronic postprocedural pain |
| G8929 | Other chronic pain |
| G893 | Neoplasm related pain (acute) (chronic) |
| G894 | Chronic pain syndrome |
| R188 | Other ascites |
| R1900 | Intra-abdominal and pelvic swelling, mass and lump, unspecified site |
| R1901 | Right upper quadrant abdominal swelling, mass and lump |
| R1902 | Left upper quadrant abdominal swelling, mass and lump |
| R1903 | Right lower quadrant abdominal swelling, mass and lump |
| R1904 | Left lower quadrant abdominal swelling, mass and lump |
| R1905 | Periumbilic swelling, mass or lump |
| R1906 | Epigastric swelling, mass or lump |
| R1907 | Generalized intra-abdominal and pelvic swelling, mass and lump |
| R1909 | Other intra-abdominal and pelvic swelling, mass and lump |
| R1930 | Abdominal rigidity, unspecified site |
| R1931 | Right upper quadrant abdominal rigidity |
| R1932 | Left upper quadrant abdominal rigidity |
| R1933 | Right lower quadrant abdominal rigidity |
| R1934 | Left lower quadrant abdominal rigidity |
| R1935 | Periumbilic abdominal rigidity |
| R1936 | Epigastric abdominal rigidity |
| R1937 | Generalized abdominal rigidity |
| R410 | Disorientation, unspecified |
| R411 | Anterograde amnesia |
| R412 | Retrograde amnesia |
| R413 | Other amnesia |
| R4182 | Altered mental status, unspecified |
| R419 | Unspecified symptoms and signs involving cognitive functions and awareness |
| R448 | Other symptoms and signs involving general sensations and perceptions |
| R449 | Unspecified symptoms and signs involving general sensations and perceptions |
| R4583 | Excessive crying of child, adolescent or adult |
| R4584 | Anhedonia |
| R460 | Very low level of personal hygiene |
| R461 | Bizarre personal appearance |
| R462 | Strange and inexplicable behavior |
| R463 | Overactivity |
| R464 | Slowness and poor responsiveness |
| R465 | Suspiciousness and marked evasiveness |
| R466 | Undue concern and preoccupation with stressful events |
| R467 | Verbosity and circumstantial detail obscuring reason for contact |
| R52 | Pain, unspecified |
| R680 | Hypothermia, not associated with low environmental temperature |
| R6811 | Excessive crying of infant (baby) |
| R6812 | Fussy infant (baby) |
| R6813 | Apparent life threatening event in infant (ALTE) |
| R6819 | Other nonspecific symptoms peculiar to infancy |
| R6881 | Early satiety |
| R6882 | Decreased libido |
| R6883 | Chills (without fever) |
| R6889 | Other general symptoms and signs |
| R69 | Illness, unspecified |
| |
| PDX Collection 1553 |
| A33 | Tetanus neonatorum |
| A35 | Other tetanus |
| G10 | Huntington's disease |
| G110 | Congenital nonprogressive ataxia |
| G1110 | Early-onset cerebellar ataxia, unspecified |
| G1111 | Friedreich ataxia |
| G1119 | Other early-onset cerebellar ataxia |
| G112 | Late-onset cerebellar ataxia |
| G114 | Hereditary spastic paraplegia |
| G20A1 | Parkinson's disease without dyskinesia, without mention of fluctuations |
| G20A2 | Parkinson's disease without dyskinesia, with fluctuations |
| G20B1 | Parkinson's disease with dyskinesia, without mention of fluctuations |
| G20B2 | Parkinson's disease with dyskinesia, with fluctuations |
| G20C | Parkinsonism, unspecified |
| G210 | Malignant neuroleptic syndrome |
| G2111 | Neuroleptic induced parkinsonism |
| G2119 | Other drug induced secondary parkinsonism |
| G212 | Secondary parkinsonism due to other external agents |
| G213 | Postencephalitic parkinsonism |
| G214 | Vascular parkinsonism |
| G218 | Other secondary parkinsonism |
| G219 | Secondary parkinsonism, unspecified |
| G230 | Hallervorden-Spatz disease |
| G231 | Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] |
| G232 | Striatonigral degeneration |
| G233 | Hypomyelination with atrophy of the basal ganglia and cerebellum |
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