Autoimmune disease Fam Mem PhenX

General Details:

Name:
Autoimmune disease Fam Mem PhenX
Steward:
LOINC
Registration Status:
Qualified

Permissible Values:

Data Type:
Value List
Unit of Measure:
Ids:
Value Code Name Code Code System Code Description
Systemic lupus erythematosus (SLE) Systemic lupus erythematosus (SLE) LA15300-9 LOINC
Rheumatoid Arthritis Rheumatoid Arthritis LA15161-5 LOINC
Sjögren’s syndrome Sjögren’s syndrome LA15301-7 LOINC
Discoid lupus Discoid lupus LA15302-5 LOINC
Autoimmune thyroid disease (AITD) Autoimmune thyroid disease (AITD) LA15303-3 LOINC
Type 1 diabetes (Juvenile onset) Type 1 diabetes (Juvenile onset) LA15304-1 LOINC
Type 2 diabetes (Adult onset) Type 2 diabetes (Adult onset) LA15305-8 LOINC
Myasthenia Gravis Myasthenia Gravis LA15158-1 LOINC
Scleroderma Scleroderma LA15306-6 LOINC
Addison's disease Addison's disease LA15307-4 LOINC
Idiopathic thrombocytopenia (ITP) Idiopathic thrombocytopenia (ITP) LA15308-2 LOINC
Antiphospholipid syndrome Antiphospholipid syndrome LA15309-0 LOINC
Graying of all hair before age 35 Graying of all hair before age 35 LA15310-8 LOINC

Designations:

Designation:
Autoimmune disease Fam Mem PhenX
Tags:
Short Name
Designation:
Autoimmune disease Family member [PhenX]
Tags:
Long Common Name
Designation:
Family History - Disease
Tags:
Question Text

Properties:

Key:
Related Names
Value:
DisDiseasesDz
Fam MemFindingFindings
NominalPoint in timeRandom
Key:
Related Codes
Value:
Code SystemCodeCode TextCode Version
https://www.phenxtoolkit.orgPX161401690100PX161401_Family_History_1_Diseasehttps://www.phenxtoolkit.orgPX161401700100PX161401_Family_History_2_Diseasehttps://www.phenxtoolkit.orgPX161401710100PX161401_Family_History_3_Disease
https://www.phenxtoolkit.orgPX161401720100PX161401_Family_History_4_Diseasehttps://www.phenxtoolkit.orgPX161401730100PX161401_Family_History_5_Diseasehttps://www.phenxtoolkit.orgPX161401740100PX161401_Family_History_6_Disease
https://www.phenxtoolkit.orgPX161401750100PX161401_Family_History_7_Diseasehttps://www.phenxtoolkit.orgPX161401760100PX161401_Family_History_8_Diseasehttps://www.phenxtoolkit.orgPX161401770100PX161401_Family_History_9_Disease
https://www.phenxtoolkit.orgPX161401780100PX161401_Family_History_10_Diseasehttps://www.phenxtoolkit.orgPX161401790100PX161401_Family_History_11_Diseasehttps://www.phenxtoolkit.orgPX161401800100PX161401_Family_History_12_Disease
https://www.phenxtoolkit.orgPX161401810100PX161401_Family_History_13_Diseasehttps://www.phenxtoolkit.orgPX161401820100PX161401_Family_History_14_Diseasehttps://www.phenxtoolkit.orgPX161401830100PX161401_Family_History_15_Disease
https://www.phenxtoolkit.orgPX161401840100PX161401_Family_History_16_Diseasehttps://www.phenxtoolkit.orgPX161401850100PX161401_Family_History_17_Disease
Key:
Fully-Specified Name
Value:
ComponentPropertyTimeSystemScaleMethod
Autoimmune diseaseFindPt^Family memberNomPhenX
Key:
Basic Attributes
Value:
ClassTypeFirst ReleasedLast UpdatedChange Reason
PHENXClinicalVersion 2.38Version 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.

Identifiers:

Source:
NLM
Id:
mJYvqinil
Version:
1.1
Source:
LOINC
Id:
66435-9
Version:
2.69