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CDE Detailed Report
This report contains detailed information about the selected CDEs.
Note: If at least one CDE was selected from a copyright- or trademark-protected instrument/scale then all of the CDEs from that instrument/scale are included in this report.
Disease: Chiari I Malformation
Sub-Domain: General Health History
CRF: CMI - Hereditary Disorder of Connective Tissue Screening (1)
Item count: 19 (19 distinct CDEs)
CDE ID
CDE Name
Variable Name
Definition / Description
Question Text
Permissible Value
Description
Data Type
Instructions
References
Population
Classification (e.g., Core)
Version #
Version Date
Aliases for Variable Name
CRF Module / Guideline
© or TM
Sub-Domain
Domain
Previous Title
Size
Input Restrictions
Min Value
Max Value
Measurement Type
LOINC ID
SNOMED
caDSR ID
CDISC ID
C01507
Blood pressure diastolic measurement
BldPressrDiastlMeasr
Measurement of pressure of the participant's/subject's blood against the artery walls during diastole (the relaxation phase) in millimeters of mercury (mmHg)
BP diastolic
  
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental
3.0
7/25/2013
SCI CDEs: BPDIAS
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
Blood pressure diastolic measurement
 
Free-Form Entry
0
300
millimeter of mercury
  
2004291
 
C01521
Heart rate
HeartRate
The participant/subject's pulse or number of contractions (heart beats) per minute
Heart rate
  
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental
3.0
8/28/2013
SCI CDEs: PULSE
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
Heart rate
 
Free-Form Entry
0
300
beats per minute
  
2767073
 
C01522
Height measurement
HgtMeasr
Measurement of participant's/subject's height.
Height measurement
  
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental
3.0
8/28/2013
SCI CDEs: HEIGHT
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
Height measurement
 
Free-Form Entry
0
400
centimeter
  
649
 
C01565
Blood pressure systolic measurement
BldPressrSystMeasr
Measurement of pressure of the participant's/subject's blood against the artery walls during systole (the contraction phase) in millimeters of mercury (mmHg)
BP systolic
  
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental
3.0
7/25/2013
SCI CDEs: BPSYS
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
Blood pressure systolic measurement
 
Free-Form Entry
0
300
millimeter of mercury
  
2004289
 
C01582
Height unit of measure
HgtUOM
Unit of measure for the height numerical value for subject/participant
Height unit of measure
  
Alphanumeric
No instructions available
No references available
Adult;Pediatric
Supplemental
3.0
7/24/2013
Aliases for variable name not defined
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
Height unit of measure
 
Single Pre-Defined Value Selected
     
2538920
 
C10724
Echocardiogram performed date and time
EchcrdgrmPerfrmDateTime
Date (and time, if applicable and known) the echocardiography was performed
Echocardiogram Date
  
Date or Date & Time
No instructions available
No references available
Adult;Pediatric
Supplemental
3.0
7/25/2013
Aliases for variable name not defined
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
Echocardiogram performed date and time
 
Free-Form Entry
       
C12175
Dual X-ray absorptiometry performed date
DEXAPerfrmDate
The date the Dual X-ray absorptiometry (DEXA) was performed
DEXA Scan Date
  
Date or Date & Time
No instructions available
No references available
Adult;Pediatric
Supplemental
3.0
7/24/2013
Aliases for variable name not defined
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
DXA performed date
 
Free-Form Entry
       
C12875
Echocardiogram mitral valve prolapse indicator
EchcrdgrmMitrlValvProlapseInd
Assessment with echocardiography of the absence or presence of prolapse of the mitral valve, often with regurgitation, associated with myxomatous proliferation of the leaflets of the mitral valve.
Mitral valve prolapsed
Yes;No;Unknown;
Yes;No;Unknown;
Alphanumeric
No instructions available
No references available
Adult;Pediatric
Supplemental–Highly Recommended
3.0
7/24/2013
Aliases for variable name not defined
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
Echocardiogram mitral valve prolapse indicator
 
Single Pre-Defined Value Selected
       
C21684
Beighton Score - Motion thumb forearm assessment score
BSMotThmbForarmAsmntScore
Score/Assessment of the motion thumb to forearm as part of the Beighton Score
Thumb to forearm
  
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental
1.0
5/26/2016
BS1
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
  
Single Pre-Defined Value Selected
       
C21685
Beighton Score - Motion finger bend back score
BSMotFngBndBckScore
Score/Assessment of Motion to bend finger back as part of the Beighton Score
Bending little fingers back 90 degrees or more
  
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental
1.0
5/26/2016
BS2
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
  
Single Pre-Defined Value Selected
       
C21686
Beighton Score - Motion elbow hyperextend score
BSMotElbHypExtScore
Score/assessment of ability to complete the motion hyperextended elbow as part of the Beighton Score
Elbows hyperextended to 10 degrees or more
  
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental
1.0
5/26/2016
BS3
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
  
Single Pre-Defined Value Selected
       
C21687
Beighton Score - Motion knee hyperextend score
BSMotKnHypExtScore
Score/assessment of ability to complete the Motion hyperextended knee as part of Beighton Score
Knees hyperextended to 10 degrees or more
  
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental
1.0
5/26/2016
BS4
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
  
Single Pre-Defined Value Selected
       
C21688
Beighton Score - Motion palm flat leg straight score
BSMotPlmFltLegStrghtScore
Score of ability of completing the motion palm flat and leg straight as part of the Beighton Score
Palms flat to floor with legs straight
0;1R;1L;
0;1 Right;1 Left;
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental
1.0
5/26/2016
BS5
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
  
Single Pre-Defined Value Selected
       
C21689
Beighton Score - Total score
BSTotalScore
Total score as related to the Beighton Score
Total score
  
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental–Highly Recommended
1.0
5/26/2016
BS6
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
  
Free-Form Entry
1
9
points
    
C22433
Medical history aortic root enlargement indicator
MedHistAorRootElargeInd
The indicator related to any medical history of the enlargement of the subject's aortic root.
Aortic root dilation
Yes;No;Unknown;
Yes;No;Unknown;
Alphanumeric
No instructions available
No references available
Adult;Pediatric
Supplemental–Highly Recommended
1.0
6/10/2016
Aliases for variable name not defined
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
  
Single Pre-Defined Value Selected
       
C22402
Hereditary disorder connective tissue diagnosis indicator
HDCTDiagnosInd
The indicator related to personal or family history of double jointedness or excessive joint flexibility or dislocations, also known as Hereditary Disorder of Connective Tissue (HDCT).
Known hereditary connective tissue disorder
Yes;No;
Yes;No;
Alphanumeric
No instructions available
No references available
Adult;Pediatric
Supplemental–Highly Recommended
1.0
6/10/2016
Aliases for variable name not defined
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
  
Single Pre-Defined Value Selected
       
C00008
Age value
AgeVal
Value for participant/subject's age, calculated as elapsed time since the birth of the participant/subject.
Age at dx
  
Numeric Values
No instructions available
No references available
Adult;Pediatric
Supplemental
3.0
8/28/2013
Aliases for variable name not defined
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
Age value
 
Free-Form Entry
0
1800
month
    
C22776
Hereditary disorder type
HereditaryDisorderTyp
The type related to hereditary disorder of connective tissues.
Assessment
Hereditary Disorders of Connective Tissue Diagnoses;Osteoarthritis/Degenerative Joint Disease;Acquired/Autoimmune Connective Tissue Disorders;Fibromyalgia Syndrome;
Hereditary Disorders of Connective Tissue Diagnoses;Osteoarthritis/Degenerative Joint Disease;Acquired/Autoimmune Connective Tissue Disorders;Fibromyalgia Syndrome;
Alphanumeric
No instructions available
No references available
Adult;Pediatric
Supplemental–Highly Recommended
1.0
10/19/2016
Aliases for variable name not defined
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
  
Multiple Pre-Defined Values Selected
       
C22775
Hereditary disorder connective tissue diagnosis type
HereDisConnTissDiagTyp
The type related to hereditary disorder of connective tissues.
Hereditary Disorders of Connective Tissue Diagnoses
Hypermobile EDS;Classical EDS;EDS – mild classical vs. hypermobile;Marfan;MASS phenotype;Stickler Syndrome;Loeys-Dietz Syndrome;Evidence of possible HDCT;Associated conditions;
Hypermobile EDS (type III – absence of skin features) “Benign joint hypermobility”;Classical EDS (type I & II – skin features);EDS – mild classical vs. hypermobile (borderline skin findings);Marfan (AS/Ht > 1.05, pectus ab, aortic dil., dural ectasia, ectopia lentis);MASS phenotype (myopia, mitral valve prolapse, aortic dil., skin & skeletal features);Stickler Syndrome (collagen type 2 or 11, myopia, hearing loss, osteoarthritis, cleft palate);Loeys-Dietz Syndrome (hypertelorism, bifid uvula, aneurysms);Evidence of possible HDCT (Unknown/Unspecified);Associated conditions;
Alphanumeric
No instructions available
No references available
Adult;Pediatric
Supplemental–Highly Recommended
1.0
10/19/2016
Aliases for variable name not defined
CMI - Hereditary Disorder of Connective Tissue Screening (1)
General Health History
Participant History and Family History
  
Multiple Pre-Defined Values Selected
       
07-20-2019
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