Do or did any of your relatives have this eye problem [PhenX]

General Details:

Name:
Do or did any of your relatives have this eye problem [PhenX]
Steward:
LOINC
Registration Status:
Qualified

Permissible Values:

Data Type:
Value List
Unit of Measure:
Ids:
Value Code Name Code Code System Code Description
1 Yes LA33-6 LOINC
2 No LA32-8 LOINC
7 Refused LA4389-8 LOINC
9 Don't know LA12688-0 LOINC

Designations:

Designation:
Do or did any of your relatives have this eye problem [PhenX]
Tags:
Long Common Name
Designation:
Relatives have eye problem PhenX
Tags:
Short Name

Properties:

Key:
Related Names
Value:
FindingFindingsOrdinal
Point in timeQLQual
QualitativeRandomRelatives have eye problem
Screen
Key:
Related Codes
Value:
Code SystemCodeCode TextCode Version
https://www.phenxtoolkit.orgPX110901090201PX110901_Glaucoma_Motherhttps://www.phenxtoolkit.orgPX110901090202PX110901_Glaucoma_Fatherhttps://www.phenxtoolkit.orgPX110901090203PX110901_Glaucoma_Sister
https://www.phenxtoolkit.orgPX110901090204PX110901_Glaucoma_Brotherhttps://www.phenxtoolkit.orgPX110901090205PX110901_Glaucoma_Daughterhttps://www.phenxtoolkit.orgPX110901090206PX110901_Glaucoma_Son
https://www.phenxtoolkit.orgPX110901090207PX110901_Glaucoma_Maternal_Grandmotherhttps://www.phenxtoolkit.orgPX110901090208PX110901_Glaucoma_Maternal_Grandfatherhttps://www.phenxtoolkit.orgPX110901090209PX110901_Glaucoma_Paternal_Grandmother
https://www.phenxtoolkit.orgPX110901090210PX110901_Glaucoma_Paternal_Grandfatherhttps://www.phenxtoolkit.orgPX110901090211PX110901_Glaucoma_Mothers_Sisterhttps://www.phenxtoolkit.orgPX110901090212PX110901_Glaucoma_Mothers_Brother
https://www.phenxtoolkit.orgPX110901090213PX110901_Glaucoma_Fathers_Sisterhttps://www.phenxtoolkit.orgPX110901090214PX110901_Glaucoma_Fathers_Brotherhttps://www.phenxtoolkit.orgPX110901090215PX110901_Glaucoma_Other_Relative
https://www.phenxtoolkit.orgPX110901110100PX110901_Macular_Degeneration_Relativehttps://www.phenxtoolkit.orgPX110901110201PX110901_Macular_Degeneration_Motherhttps://www.phenxtoolkit.orgPX110901110202PX110901_Macular_Degeneration_Father
https://www.phenxtoolkit.orgPX110901110203PX110901_Macular_Degeneration_Sisterhttps://www.phenxtoolkit.orgPX110901110204PX110901_Macular_Degeneration_Brotherhttps://www.phenxtoolkit.orgPX110901110205PX110901_Macular_Degeneration_Daughter
https://www.phenxtoolkit.orgPX110901110206PX110901_Macular_Degeneration_Sonhttps://www.phenxtoolkit.orgPX110901110207PX110901_Macular_Degeneration_Maternal_Grandmotherhttps://www.phenxtoolkit.orgPX110901110208PX110901_Macular_Degeneration_Maternal_Grandfather
https://www.phenxtoolkit.orgPX110901110209PX110901_Macular_Degeneration_Paternal_Grandmotherhttps://www.phenxtoolkit.orgPX110901110210PX110901_Macular_Degeneration_Paternal_Grandfatherhttps://www.phenxtoolkit.orgPX110901110211PX110901_Macular_Degeneration_Mothers_Sister
https://www.phenxtoolkit.orgPX110901110212PX110901_Macular_Degeneration_Mothers_Brotherhttps://www.phenxtoolkit.orgPX110901110213PX110901_Macular_Degeneration_Fathers_Sisterhttps://www.phenxtoolkit.orgPX110901110214PX110901_Macular_Degeneration_Fathers_Brother
https://www.phenxtoolkit.orgPX110901110215PX110901_Macular_Degeneration_Other_Relative
Key:
Fully-Specified Name
Value:
ComponentPropertyTimeSystemScaleMethod
Do or did any of your relatives have this eye problemFindPt^PatientOrdPhenX
Key:
Basic Attributes
Value:
ClassTypeFirst ReleasedLast UpdatedChange Reason
PHENXClinicalVersion 2.36Version 2.65Updated the PhenX ID from "PhenX." to "PX" in Survey Question Source field to align with the variable identifier used in the PhenX Toolkit.
Key:
Third Party Copyright
Value:
This material includes SNOMED Clinical Terms® (SNOMED CT®) which is used by permission of the International Health Terminology Standards Development Organisation (IHTSDO) under license. All rights reserved. SNOMED CT® was originally created by The College of American Pathologists. "SNOMED" and "SNOMED CT" are registered trademarks of the IHTSDO. This material includes content from the US Edition to SNOMED CT, which is developed and maintained by the U.S. National Library of Medicine and is available to authorized UMLS Metathesaurus Licensees from the UTS Downloads site at https://uts.nlm.nih.gov. Use of SNOMED CT content is subject to the terms and conditions set forth in the SNOMED CT Affiliate License Agreement. It is the responsibility of those implementing this product to ensure they are appropriately licensed and for more information on the license, including how to register as an Affiliate Licensee, please refer to http://www.snomed.org/snomed-ct/get-snomed-ct or info@snomed.org<mailto:info@snomed.org>. This may incur a fee in SNOMED International non-Member countries.
Key:
LOINC Copyright
Value:
This material includes SNOMED Clinical Terms® (SNOMED CT®) which is used by permission of the International Health Terminology Standards Development Organisation (IHTSDO) under license. All rights reserved. SNOMED CT® was originally created by The College of American Pathologists. "SNOMED" and "SNOMED CT" are registered trademarks of the IHTSDO. This material includes content from the US Edition to SNOMED CT, which is developed and maintained by the U.S. National Library of Medicine and is available to authorized UMLS Metathesaurus Licensees from the UTS Downloads site at https://uts.nlm.nih.gov. Use of SNOMED CT content is subject to the terms and conditions set forth in the SNOMED CT Affiliate License Agreement. It is the responsibility of those implementing this product to ensure they are appropriately licensed and for more information on the license, including how to register as an Affiliate Licensee, please refer to http://www.snomed.org/snomed-ct/get-snomed-ct or info@snomed.org<mailto:info@snomed.org>. This may incur a fee in SNOMED International non-Member countries.

Identifiers:

Source:
NLM
Id:
mJutv5jhie
Version:
1.1
Source:
LOINC
Id:
65673-6
Version:
2.69