Code System Concept

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Code System Concept

Code System Concept Code	276426004
Code System Concept Name	Ornithine oxo-acid aminotransferase deficiency (disorder)
Code System Preferred Concept Name	Ornithine oxo-acid aminotransferase deficiency (disorder)
Concept Status	Published
Concept Status Date	09/01/2024
Code System Name	SNOMED-CT

Concept Relationships
Concept Details

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Superseded By Concept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
2476096010	Deficiency of ornithine-oxo-acid aminotransferase	Active	Synonym	false	false
2669599018	Ornithine oxo-acid aminotransferase deficiency	Active	Synonym	false	false
412550019	Ornithine aminotransferase deficiency	Active	Synonym	false	false
412551015	Ornithine ketoacid transaminase deficiency	Active	Synonym	false	false
412552010	OKT deficiency	Active	Synonym	false	false
412553017	Ornithine-oxo-acid amino acid transferase deficiency	Active	Synonym	false	false
412554011	Ornithine-delta-aminotransferase deficiency	Active	Synonym	false	false
412555012	OAT - Ornithine oxo-acid aminotransferase deficiency	Active	Synonym	false	false
412556013	OAT deficiency	Active	Synonym	false	false

Associated Value Sets

Value Set Name	Version(s)
Birth Defect Diagnosis	1
Clinical Finding (NNDSS)	2 , 1
Disease	10 , 9 , 8 , 7 , 6 , 5 , 4 , 3 , 2 , 1
Problem Value Set	3 , 2

Parent Concepts Parent Concepts Parent/Child (Relationship Type) Deficiency of transferase (disorder) {124237001 , SNOMED-CT } Disorder of ornithine metabolism (disorder) {237928008 , SNOMED-CT }	Other Relationships No other relationships present.
Child Concepts Ornithine oxo-acid aminotransferase deficiency (disorder) {276426004 , SNOMED-CT } Parent/Child (Relationship Type) Ornithinemia with gyrate atrophy (disorder) {314466003 , SNOMED-CT }

Page last reviewed:June 20, 2024
Page last updated:June 20, 2024
Content source:
- Centers for Disease Control and Prevention,