Application Version: 4.0.6.10
Content Version: 2024.07.12
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Code System Concept
Code System Concept Code | 58610003 |
Code System Concept Name | Leber's optic atrophy (disorder) |
Code System Preferred Concept Name | Leber's optic atrophy (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Superseded By Concept | |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 |
---|---|---|---|---|---|
1231857010 | Leber hereditary optic neuropathy | Active | Synonym | false | false |
1231858017 | LHON - Leber hereditary optic neuropathy | Active | Synonym | false | false |
1231859013 | LHON - Leber's hereditary optic neuropathy | Active | Synonym | false | false |
2839596015 | Leber optic atrophy | Active | Synonym | false | false |
97397016 | Leber's optic atrophy | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
Congenital anomaly of head (disorder)
{87290003
, SNOMED-CT
}
Congenital anomaly of skeletal muscle (disorder)
{89886004
, SNOMED-CT
}
Degenerative disorder of musculoskeletal system (disorder)
{363059001
, SNOMED-CT
}
Disorder of pyruvate metabolism and mitochondrial respiratory chain (disorder)
{237981000
, SNOMED-CT
}
Hereditary disorder of musculoskeletal system (disorder)
{363212003
, SNOMED-CT
}
Hereditary optic atrophy (disorder)
{26360005
, SNOMED-CT
}
Inherited metabolic disorder of nervous system (disorder)
{128190004
, SNOMED-CT
}
Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder)
{1162975000
, SNOMED-CT
}
Mitochondrial cytopathy (disorder)
{240096000
, SNOMED-CT
}
|
Other Relationships
No other relationships present.
|
Child Concepts
Leber's optic atrophy (disorder) {58610003 , SNOMED-CT }
Parent/Child (Relationship Type)
|
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: