Application Version: 4.0.6.10
Content Version: 2024.07.12
Release Notes [PDF288KB]
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Code System Concept
Code System Concept Code | 28821000119102 |
Code System Concept Name | Lysosomal storage disease (disorder) |
Code System Preferred Concept Name | Lysosomal storage disease (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Superseded By Concept | |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 | 03/01/2024 |
SDO Date Created | 07/31/2023 |
SDO Date Revised | 07/31/2023 |
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 |
---|---|---|---|---|---|
5234013014 | Lysosomal storage disease | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
|
Other Relationships
No other relationships present.
|
Child Concepts
Lysosomal storage disease (disorder) {28821000119102 , SNOMED-CT }
Parent/Child (Relationship Type)
Cystinosis (disorder)
{190681003
, SNOMED-CT
}
Disorder of sialic acid metabolism (disorder)
{238050009
, SNOMED-CT
}
Gangliosidosis (disorder)
{50967008
, SNOMED-CT
}
Glycogen storage disease due to lysosomal associated membrane protein 2 deficiency (disorder)
{419097006
, SNOMED-CT
}
Lysosomal acid lipase deficiency (disorder)
{715923003
, SNOMED-CT
}
Mucolipidosis (disorder)
{70528007
, SNOMED-CT
}
Mucopolysaccharidosis (disorder)
{11380006
, SNOMED-CT
}
Neuronal ceroid lipofuscinosis (disorder)
{42012007
, SNOMED-CT
}
Oligosaccharidosis (disorder)
{1155842003
, SNOMED-CT
}
Sphingolipidosis (disorder)
{238028008
, SNOMED-CT
}
|
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: