Application Version: 4.0.6.10
Content Version: 2024.07.12
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Code System Concept
Code System Concept Code | 7265005 |
Code System Concept Name | Glycogen storage disease, type I (disorder) |
Code System Preferred Concept Name | Glycogen storage disease, type I (disorder) |
Concept Status | Published |
Concept Status Date | 09/01/2024 |
Code System Name | SNOMED-CT |
Concept Details
Code System Code | PH_SNOMED-CT |
Code System OID | 2.16.840.1.113883.6.96 |
HL7 Table 0396 Code | SCT |
Superseded By Concept | |
SDO Concept Status | Active |
SDO Concept Status Date | 01/31/2002 |
SDO Date Created | 01/31/2002 |
SDO Date Revised | 01/31/2002 |
Description | |
Sequence |
Extended Properties
No extended properties.
Concept Alternate Designations
SDO Designation ID | Concept Designation Description | Status | Designation Type | PHIN Preferred Term Flag | Code Flag |
---|---|---|---|---|---|
12994015 | Glycogen storage disease, type I | Active | Synonym | false | false |
12995019 | Hepatorenal glycogen storage disease | Active | Synonym | false | false |
12996018 | Glucose-6-phosphatase deficiency | Active | Synonym | false | false |
12997010 | von Gierke's disease | Active | Synonym | false | false |
12998017 | GSD I | Active | Synonym | false | false |
3037037019 | Glycogen storage disease, type 1 | Active | Synonym | false | false |
502178014 | Liver glycogen disease | Active | Synonym | false | false |
502179018 | von Gierke disease | Active | Synonym | false | false |
502180015 | Glycogen storage disease type Ia | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
Autosomal recessive hereditary disorder (disorder)
{85995004
, SNOMED-CT
}
Congenital anomaly of abdomen (disorder)
{363024001
, SNOMED-CT
}
Congenital anomaly of body cavity (disorder)
{363026004
, SNOMED-CT
}
Congenital anomaly of digestive organ (disorder)
{128332003
, SNOMED-CT
}
Congenital anomaly of digestive system (disorder)
{69518005
, SNOMED-CT
}
Congenital anomaly of liver (disorder)
{89166001
, SNOMED-CT
}
Congenital anomaly of skeletal muscle (disorder)
{89886004
, SNOMED-CT
}
Congenital anomaly of trunk (disorder)
{78626001
, SNOMED-CT
}
Glycogen storage disease (disorder)
{29633007
, SNOMED-CT
}
Glycogen storage disease, hepatic form (disorder)
{6075009
, SNOMED-CT
}
Lesion of liver (disorder)
{300331000
, SNOMED-CT
}
|
Other Relationships
No other relationships present.
|
Child Concepts
Glycogen storage disease, type I (disorder) {7265005 , SNOMED-CT } |
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: