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 | 74370006 |
Code System Concept Name | Micromelia (disorder) |
Code System Preferred Concept Name | Micromelia (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Superseded By Concept | |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 | 07/31/2002 |
SDO Date Created | 01/31/2002 |
SDO Date Revised | 07/31/2002 |
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 |
---|---|---|---|---|---|
123510010 | Micromelia | Active | Synonym | false | false |
123512019 | Micromelus | Active | Synonym | false | false |
123513012 | Micromelic dwarf | Active | Synonym | false | false |
123515017 | Nanomelia | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
|
Other Relationships
No other relationships present.
|
Child Concepts
Micromelia (disorder) {74370006 , SNOMED-CT }
Parent/Child (Relationship Type)
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome (disorder)
{1229999001
, SNOMED-CT
}
Diastrophic dysplasia (disorder)
{58561002
, SNOMED-CT
}
Microlissencephaly micromelia syndrome (disorder)
{723405001
, SNOMED-CT
}
Micromelic dwarfism Fryn type (disorder)
{1003371001
, SNOMED-CT
}
Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder)
{770679002
, SNOMED-CT
}
Short rib polydactyly syndrome type I (disorder)
{726032008
, SNOMED-CT
}
Short rib polydactyly syndrome type V (disorder)
{1279843003
, SNOMED-CT
}
|
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: