| 82237-9 |
Total score |
Score |
^Patient |
Pt |
Qn |
NDI |
|
ACTIVE |
Total score [NDI] |
|
ADD |
DefinitionDescription |
|
|
score |
|
This article was published in the JOURNAL OF MANIPULATIVE AND PHYSIOLOGICAL THERAPEUTICS, vol14(7) Vernon, H. and Mior, S., The Neck Disability Index: a study of reliability and validity, pp.409 to 415, Copyright �© Elsevier (1991) Used with permission |
|
|
|
|
SURVEY.GNHLTH |
|
82237-9 |
|
NDI |
|
|
Both |
|
|
|
0 |
|
|
|
|
|
|
Point in time; QNT; Quan; Quant; Quantitative; Random; Scale; Survey; SURVEY.GNHLTH; Tot; Totl |
2.56 |
2.56 |
|
|
|
|
This article was published in the JOURNAL OF MANIPULATIVE AND PHYSIOLOGICAL THERAPEUTICS, vol14(7) Vernon, H. and Mior, S., The Neck Disability Index: a study of reliability and validity, pp.409 to 415, Copyright �© Elsevier (1991) Used with permission |
|
|
{score} |
|
|
|
0 |
| 82238-7 |
Chromosome region 15q11-13 deletion+duplication |
Find |
Amnio fld/CVS |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 15q11-13 deletion and duplication mutation analysis in Amniotic fluid or Chorionic villus sample by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82238-7 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 15q11-13 Del+Dup Amn/CVS FISH |
|
|
|
|
|
AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Amplification; Angelman + Prader Willi syndrome; Angelman syndrome; AWS; Chorionic villi; Chorionic villus sample; Chr 15q11-13; Chr 15q11-13 deletion+duplication; Chromosom; Chromosomes; Cyto loc; Del; Del+Dup; Deletions; Document; Dp; Finding; Findings; Fluorescent in situ hybridization; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; OB; ObGyn; Obstetrics; Point in time; Prader Willi syndrome; Random |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82239-5 |
Chromosome region 16p13.3 deletion |
Find |
Bld/Tiss |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 16p13.3 deletion in Blood or Tissue by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82239-5 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 16p13.3 Del Bld/T FISH |
|
|
|
|
|
Blood; Chr 16p13.3; Chr 16p13.3 deletion; Chromosom; Chromosomes; CREB Binding Protein; CREBBP; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Point in time; Random; Rubinstein-Taybi syndrome; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 8224-8 |
Opiates |
PrThr |
Unk sub |
Pt |
Ord |
|
|
ACTIVE |
Opiates [Presence] in Unknown substance |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
DRUG/TOX |
|
8224-8 |
|
|
|
|
Both |
|
|
|
0 |
Opiates Usub Ql |
|
|
|
|
|
Addiction; DRUG/TOXICOLOGY; Drugs; Drugs of abuse; Heroin; Illicit; OP; Opi; Opiate; Ordinal; Point in time; PotentialForAbuse; PR; QL; Qual; Qualitative; Random; Screen; Unknown substance; Usub |
2.56 |
1.0h(2) |
|
|
|
|
|
|
|
|
|
|
The Property has been changed from ACnc to reflect the new model for ordinal terms where results are based on a cut-off value.; The PrThr property is used for LOINC terms whose results are reported using an ordered categorical scale, regardless of whether or not an internal threshold was used to make that determination. This change was approved by the Laboratory LOINC Committee in June 2016. |
0 |
| 82240-3 |
Chromosome region 16p13.3 deletion |
Find |
Amnio fld/CVS |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 16p13.3 deletion in Amniotic fluid or Chorionic villus sample by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82240-3 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 16p13.3 Del Amn/CVS FISH |
|
|
|
|
|
AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Chorionic villi; Chorionic villus sample; Chr 16p13.3; Chr 16p13.3 deletion; Chromosom; Chromosomes; CREB Binding Protein; CREBBP; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; OB; ObGyn; Obstetrics; Point in time; Random; Rubinstein-Taybi syndrome |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82241-1 |
Chromosome region 17p11.2 deletion |
Find |
Amnio fld/CVS |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 17p11.2 deletion in Amniotic fluid or Chorionic villus sample by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82241-1 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 17p11.2 Del Amn/CVS FISH |
|
|
|
|
|
AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Chorionic villi; Chorionic villus sample; Chr 17p11.2; Chr 17p11.2 deletion; Chromosom; Chromosomes; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; OB; ObGyn; Obstetrics; Point in time; Potocki-Lupski syndrome; PTLS; RAI1; Random; Smith-Magenis syndrome |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82242-9 |
Chromosome region 17p13.3 deletion |
Find |
Amnio fld/CVS |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 17p13.3 deletion in Amniotic fluid or Chorionic villus sample by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82242-9 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 17p13.3 Del Amn/CVS FISH |
|
|
|
|
|
AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Chorionic villi; Chorionic villus sample; Chr 17p13.3; Chr 17p13.3 deletion; Chromosom; Chromosome 17p13.3 duplication syndrome; Chromosomes; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Miller-Dieker lissencephaly syndrome; Molecular pathology; MOLPATH; MOLPATH.DELDUP; OB; ObGyn; Obstetrics; Point in time; Random |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82243-7 |
Chromosome region 17p13.3 deletion |
Find |
Bld/Tiss |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 17p13.3 deletion in Blood or Tissue by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82243-7 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 17p13.3 Del Bld/T FISH |
|
|
|
|
|
Blood; Chr 17p13.3; Chr 17p13.3 deletion; Chromosom; Chromosome 17p13.3 duplication syndrome; Chromosomes; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; Miller-Dieker lissencephaly syndrome; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82244-5 |
Chromosome region 1p36 deletion |
Find |
Bld/Tiss |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 1p36 deletion in Blood or Tissue by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82244-5 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 1p36 Del Bld/T FISH |
|
|
|
|
|
1p36 deletion syndrome; Blood; Chr 1p36; Chr 1p36 deletion; Chromosom; Chromosomes; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82245-2 |
Chromosome region 22q11.2 deletion+duplication |
Find |
Amnio fld/CVS |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 22q11.2 deletion and duplication mutation analysis in Amniotic fluid or Chorionic villus sample by FISH |
|
NAM |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82245-2 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 22q11.2 Del+Dup Amn/CVS FISH |
|
|
|
|
|
AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Amplification; CATCH22; Chorionic villi; Chorionic villus sample; Chr 22q11.2; Chr 22q11.2 deletion; Chromosom; Chromosomes; Cyto loc; Del; Del+Dup; Deletions; DiGeorge Syndrome; Document; Dp; Finding; Findings; Fluorescent in situ hybridization; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; OB; ObGyn; Obstetrics; Point in time; Random; Velo Cardio Facial Syndrome |
2.67 |
2.56 |
|
|
|
|
|
|
|
|
|
|
Release 2.67: COMPONENT: Updated Component to reflect that a FISH study can detect deletions and duplications. |
0 |
| 82246-0 |
Chromosome region 22q11.2 deletion+duplication |
Find |
Bld/Tiss |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 22q11.2 deletion and duplication mutation analysis in Blood or Tissue by FISH |
|
NAM |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82246-0 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 22q11.2 Del+Dup Bld/T FISH |
|
|
|
|
|
Amplification; Blood; CATCH22; Chr 22q11.2; Chr 22q11.2 deletion; Chromosom; Chromosomes; Cyto loc; Del; Del+Dup; Deletions; DiGeorge Syndrome; Document; Dp; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Point in time; Random; Tissue; Tissue, unspecified; Velo Cardio Facial Syndrome; WB; Whole blood; Whole blood or Tissue |
2.67 |
2.56 |
|
|
|
|
|
|
|
|
|
|
Release 2.67: COMPONENT: Updated the Component to reflect that the FISH study can detect deletions and duplications. |
0 |
| 82247-8 |
Chromosome region 7q11.23 deletion |
Find |
Amnio fld/CVS |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 7q11.23 deletion in Amniotic fluid or Chorionic villus sample by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82247-8 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 7q11.23 Del Amn/CVS FISH |
|
|
|
|
|
AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Chorionic villi; Chorionic villus sample; Chr 7q11.23; Chr 7q11.23 deletion; Chromosom; Chromosomes; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; OB; ObGyn; Obstetrics; Point in time; Random; Williams Beuren Syndrome |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82248-6 |
Chromosome region 7q11.23 deletion |
Find |
Bld/Tiss |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 7q11.23 deletion in Blood or Tissue by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82248-6 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 7q11.23 Del Bld/T FISH |
|
|
|
|
|
Blood; Chr 7q11.23; Chr 7q11.23 deletion; Chromosom; Chromosomes; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue; Williams Beuren Syndrome |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82249-4 |
Chromosome region 8q23.3-24.13 deletion |
Find |
Bld/Tiss |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 8q23.3-24.13 deletion in Blood or Tissue by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82249-4 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 8q23.3-24.13 Del Bld/T FISH |
|
|
|
|
|
Blood; Chr 8q23.3-24.13; Chr 8q23.3-24.13 deletion; Chromosom; Chromosomes; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; Langer Giedion Syndrome; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Point in time; Random; Tissue; Tissue, unspecified; Trichorhinophalangeal syndrome 1; Trichorhinophalangeal syndrome 2; TRPS2; WB; Whole blood; Whole blood or Tissue |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 8225-5 |
Opiates |
PrThr |
Unk sub |
Pt |
Ord |
Confirm |
|
ACTIVE |
Opiates [Presence] in Unknown substance by Confirmatory method |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
DRUG/TOX |
|
8225-5 |
|
Confirm |
|
|
Both |
|
|
|
0 |
Opiates Usub Ql Cfm |
|
|
|
|
|
Addiction; Cfm; CNFR; CNFRM; Conf; Confirmation; Confirmatory; DRUG/TOXICOLOGY; Drugs; Drugs of abuse; GCMS; Heroin; Illicit; LC/MS/MS; OP; Opi; Opiate; Ordinal; Point in time; PotentialForAbuse; PR; QL; Qual; Qualitative; Random; Screen; Unknown substance; Usub |
2.56 |
1.0h(2) |
|
|
|
|
|
|
|
|
|
|
The Property has been changed from ACnc to reflect new model for ordinal terms; The PrThr property is used for LOINC terms whose results are reported using an ordered categorical scale, regardless of whether or not an internal threshold was used to make that determination. This change was approved by the Laboratory LOINC Committee in June 2016. |
0 |
| 82250-2 |
Chromosome region 1p subtelomere & 1p36 deletion & 1q25 rearrangement |
Find |
Bld/Tiss |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome region 1p subtelomere and 1p36 deletion and 1q25 rearrangement in Blood or Tissue by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.MISC |
|
82250-2 |
|
FISH |
|
|
Both |
|
|
|
0 |
1p tel+1p36 del + 1q25 rearr Bld/T FISH |
|
|
|
|
|
1p tel+1p36 del + 1q25 rearr; Blood; Chromosom; Chromosomes; Cyto loc; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; MISC; Miscellaneous molecular pathology; Molecular pathology; MOLPATH; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82251-0 |
Chromosome 3 & 7 & 17 aneuploidy & chromosome region 9p21 deletion |
Find |
Urine |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome 3 and 7 and 17 aneuploidy and chromosome region 9p21 deletion in Urine by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.MISC |
|
82251-0 |
|
FISH |
|
|
Both |
|
|
|
0 |
Chr 3+7+17 aneu + 9p21 Del Ur FISH |
|
|
|
|
|
Bladder Cancers; Bladder cell cancer; Bladder Tumor; Chr 3 + 7 + 17 aneup + Chr 9p21 del; Chr 3+7+17 aneu + 9p21; Chromosom; Chromosomes; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; III; Inherited; MISC; Miscellaneous molecular pathology; Molecular pathology; MOLPATH; Point in time; Random; UA; UR; Urn |
2.73 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82252-8 |
Constitutive heterochromatin analysis |
Find |
Bld/Tiss |
Pt |
Doc |
Banding |
|
ACTIVE |
Constitutive heterochromatin analysis in Blood or Tissue by Banding |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.MISC |
|
82252-8 |
|
Banding |
|
|
Both |
|
|
|
0 |
Cons heterochrom analysis Bld/T Banding |
|
|
|
|
|
Blood; Cons heterochromatin analysis; Document; Finding; Findings; Genetics; Heredity; Heritable; Inherited; MISC; Miscellaneous molecular pathology; Molecular pathology; MOLPATH; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82253-6 |
JAG1 gene deletion |
Find |
Bld/Tiss |
Pt |
Doc |
FISH |
|
ACTIVE |
JAG1 gene deletion in Blood or Tissue by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82253-6 |
|
FISH |
|
|
Both |
|
|
|
0 |
JAG1 gene Del Bld/T FISH |
|
|
|
|
|
AGS; AHD; Alagille syndrome; AWS; Blood; CD339; CD339 antigen; Chromosome 20p12.1-p11.23; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; HJ1; Inherited; jagged 1; Jagged1; Jagged-1 precursor; JAGL1; MGC104644; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Point in time; Random; Tissue; Tissue, unspecified; ToF; WB; Whole blood; Whole blood or Tissue |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82254-4 |
Marker & derivative chromosome analysis |
Find |
Amnio fld/CVS |
Pt |
Doc |
Cytogenetics |
|
ACTIVE |
Marker and derivative chromosome analysis in Amniotic fluid or Chorionic villus sample Document by Cytogenetics |
|
ADD |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
CYTO |
|
82254-4 |
|
Cytogenetics |
|
|
Both |
|
|
|
0 |
Mar + der chrom analy Amn/CVS Doc |
|
|
|
|
|
AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Chorionic villi; Chorionic villus sample; Chrom analy; Chromosom; Chromosomes; Cytog; Cytogenetics; CYTOLOGY; Document; Finding; Findings; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Karyotype; Mar + der chrom analy; Mark; OB; ObGyn; Obstetrics; Point in time; Random |
2.56 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82255-1 |
Marker & derivative chromosome analysis |
Find |
Bld/Tiss |
Pt |
Doc |
Cytogenetics |
|
ACTIVE |
Marker and derivative chromosome analysis in Blood or Tissue Document by Cytogenetics |
|
ADD |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
CYTO |
|
82255-1 |
|
Cytogenetics |
|
|
Both |
|
|
|
0 |
Mar + der chrom analy Bld/T Doc |
|
|
|
|
|
Blood; Chrom analy; Chromosom; Chromosomes; Cytog; Cytogenetics; CYTOLOGY; Document; Finding; Findings; Genetics; Heredity; Heritable; Inherited; Karyotype; Mar + der chrom analy; Mark; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue |
2.56 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82256-9 |
Chromosome 12 trisomy & chromosome region 11q22.3 & 13q14 & 17p13.1 deletion |
Find |
Bld/Tiss |
Pt |
Doc |
FISH |
|
ACTIVE |
Chromosome 12 trisomy and chromosome region 11q22.3 and 13q14 and 17p13.1 deletion in Blood or Tissue by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.MISC |
|
82256-9 |
|
FISH |
|
|
Both |
|
|
|
0 |
12Ts+11p22.3+13q14+17p13.1 Del Bl/T FISH |
|
|
|
|
|
Blood; Chr 12 Ts; Chr 12 Ts + Chr 11q22.3 + 13q14 + 17p13.1 del; Chr 12Ts + 11q22.3+13q14+17p13.1; Chromosom; Chromosomes; Chronic lymphocytic leukemia; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; MISC; Miscellaneous molecular pathology; Molecular pathology; MOLPATH; Point in time; Random; Tissue; Tissue, unspecified; Ts; WB; Whole blood; Whole blood or Tissue |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
Changed "11p22.3" in Component to "11q22.3", the correct location (long arm of the chromosome). |
0 |
| 82257-7 |
SRY gene deletion |
Find |
Bld/Tiss |
Pt |
Doc |
FISH |
|
ACTIVE |
SRY gene deletion in Blood or Tissue by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.DELDUP |
|
82257-7 |
|
FISH |
|
|
Both |
|
|
|
0 |
SRY gene Del Bld/T FISH |
|
|
|
|
|
Blood; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Gonadal Dysgenesis, 46, XY; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Point in time; Random; Sex determining region Y; SRXX1; SRXY1; Swyer James Syndrome; TDF; TDY; Testis determining factor; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
|
0 |
| 82258-5 |
Subtelomere analysis |
Find |
Bone mar |
Pt |
Doc |
FISH |
|
ACTIVE |
Subtelomere analysis in Bone marrow by FISH |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
MOLPATH.MISC |
|
82258-5 |
|
FISH |
|
|
Both |
|
|
|
0 |
Subtelomere analysis Mar FISH |
|
|
|
|
|
BM; BON; Bone marrow; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; MAR; Marrow (bone); minimal angle of resolution; Minimum angle of resolution; MISC; Miscellaneous molecular pathology; Molecular pathology; MOLPATH; Point in time; Random |
2.65 |
2.56 |
|
|
|
|
|
|
|
|
|
|
Updated System from "Bone marrow" to "Bone mar" to be consistent with other laboratory bone marrow terms. |
0 |
| 82259-3 |
Metabolic equivalent of task & Resting metabolic rate panel |
- |
^Patient |
Pt |
- |
|
|
ACTIVE |
Metabolic equivalent of task and Resting metabolic rate panel |
|
MIN |
DefinitionDescription |
|
|
|
|
|
|
|
|
|
PANEL.CLIN |
|
82259-3 |
|
|
|
|
Order |
|
|
|
0 |
MET + RMR Pnl |
|
|
|
|
|
Basal Metabolic Rate; BMR; CLIN; EE; Energy expenditure; MET + RMR Pnl; Pan; PANEL.CLINICAL; Panl; Pnl; Point in time; Random; RMR; RMR Pnl |
2.71 |
2.56 |
|
Convenience group |
|
|
|
|
|
|
|
|
|
0 |
