PDX Collection 1116 (continued) |
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 |
Q998 | Other specified chromosome abnormalities |
Q999 | Chromosomal abnormality, unspecified |
|
PDX Collection 1117 |
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 |
Q933 | Deletion of short arm of chromosome 4 |
Q934 | Deletion of short arm of chromosome 5 |
Q9351 | Angelman syndrome |
Q9359 | Other deletions of part of a chromosome |
Q937 | Deletions with other complex rearrangements |
Q9381 | Velo-cardio-facial syndrome |
Q9382 | Williams syndrome |
Q9388 | Other microdeletions |
Q9389 | Other deletions from the autosomes |
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 |
Q998 | Other specified chromosome abnormalities |
Q999 | Chromosomal abnormality, unspecified |
|
PDX Collection 1118 |
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 |
Q933 | Deletion of short arm of chromosome 4 |
Q934 | Deletion of short arm of chromosome 5 |
Q9351 | Angelman syndrome |
Q9359 | Other deletions of part of a chromosome |
Q937 | Deletions with other complex rearrangements |
Q9381 | Velo-cardio-facial syndrome |
Q9382 | Williams syndrome |
Q9388 | Other microdeletions |
Q9389 | Other deletions from the autosomes |
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 |
Q998 | Other specified chromosome abnormalities |
Q999 | Chromosomal abnormality, unspecified |
|
PDX Collection 1119 |
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 1121 |
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 |
R29700 | NIHSS score 0 |
R29701 | NIHSS score 1 |
R29702 | NIHSS score 2 |
R29703 | NIHSS score 3 |
R29704 | NIHSS score 4 |
R29705 | NIHSS score 5 |
R29706 | NIHSS score 6 |
R29707 | NIHSS score 7 |
R29708 | NIHSS score 8 |
R29709 | NIHSS score 9 |
R29710 | NIHSS score 10 |
R29711 | NIHSS score 11 |
R29712 | NIHSS score 12 |
R29713 | NIHSS score 13 |
R29714 | NIHSS score 14 |
R29715 | NIHSS score 15 |
R29716 | NIHSS score 16 |
R29717 | NIHSS score 17 |
R29718 | NIHSS score 18 |
R29719 | NIHSS score 19 |
R29720 | NIHSS score 20 |
R29721 | NIHSS score 21 |
R29722 | NIHSS score 22 |
R29723 | NIHSS score 23 |
R29724 | NIHSS score 24 |
R29725 | NIHSS score 25 |
R29726 | NIHSS score 26 |
R29727 | NIHSS score 27 |
R29728 | NIHSS score 28 |
R29729 | NIHSS score 29 |
R29730 | NIHSS score 30 |
R29731 | NIHSS score 31 |
R29732 | NIHSS score 32 |
R29733 | NIHSS score 33 |
R29734 | NIHSS score 34 |
R29735 | NIHSS score 35 |
R29736 | NIHSS score 36 |
R29737 | NIHSS score 37 |
R29738 | NIHSS score 38 |
R29739 | NIHSS score 39 |
R29740 | NIHSS score 40 |
R29741 | NIHSS score 41 |
R29742 | NIHSS score 42 |
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 |
R4681 | Obsessive-compulsive behavior |
R4689 | Other symptoms and signs involving appearance and behavior |
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 1122 |
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 1123 |
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 |
R180 | Malignant ascites |
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 |
R29700 | NIHSS score 0 |
R29701 | NIHSS score 1 |
R29702 | NIHSS score 2 |
R29703 | NIHSS score 3 |
R29704 | NIHSS score 4 |
R29705 | NIHSS score 5 |
R29706 | NIHSS score 6 |
R29707 | NIHSS score 7 |
R29708 | NIHSS score 8 |
R29709 | NIHSS score 9 |
R29710 | NIHSS score 10 |
R29711 | NIHSS score 11 |
R29712 | NIHSS score 12 |
R29713 | NIHSS score 13 |
R29714 | NIHSS score 14 |
R29715 | NIHSS score 15 |
R29716 | NIHSS score 16 |
R29717 | NIHSS score 17 |
R29718 | NIHSS score 18 |
R29719 | NIHSS score 19 |
R29720 | NIHSS score 20 |
R29721 | NIHSS score 21 |
R29722 | NIHSS score 22 |
R29723 | NIHSS score 23 |
R29724 | NIHSS score 24 |
R29725 | NIHSS score 25 |
R29726 | NIHSS score 26 |
R29727 | NIHSS score 27 |
R29728 | NIHSS score 28 |
R29729 | NIHSS score 29 |
R29730 | NIHSS score 30 |
R29731 | NIHSS score 31 |
R29732 | NIHSS score 32 |
R29733 | NIHSS score 33 |
R29734 | NIHSS score 34 |
R29735 | NIHSS score 35 |
R29736 | NIHSS score 36 |
R29737 | NIHSS score 37 |
R29738 | NIHSS score 38 |
R29739 | NIHSS score 39 |
R29740 | NIHSS score 40 |
R29741 | NIHSS score 41 |
R29742 | NIHSS score 42 |
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 |
R4681 | Obsessive-compulsive behavior |
R4689 | Other symptoms and signs involving appearance and behavior |
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 1124 |
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 |
G20 | Parkinson's disease |
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 |