Code System Concept

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Code System Concept

Code System Concept Code	234363001
Code System Concept Name	Selective malabsorption of cyanocobalamin (disorder)
Code System Preferred Concept Name	Selective malabsorption of cyanocobalamin (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Superseded By Concept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
1783502019	Vitamin B12 deficiency anaemia due to selective malabsorption of cyanocobalamin	Active	Synonym	false	false
1783871017	Vitamin B12 deficiency anemia due to selective malabsorption of cyanocobalamin	Active	Synonym	false	false
351109018	Imerslund-Grasbeck anemia	Active	Synonym	false	false
351110011	Selective malabsorption of cyanocobalamin	Active	Synonym	false	false
351111010	Imerslund-Grasbeck anaemia	Active	Synonym	false	false
351112015	Congenital vitamin B12 deficiency	Active	Synonym	false	false
351113013	Imerslund-Najman-Grasbeck syndrome	Active	Synonym	false	false
351114019	Imerslund-Grasbeck disease	Active	Synonym	false	false
351115018	Imerslund-Grasbeck syndrome	Active	Synonym	false	false
351116017	Imerslund disease	Active	Synonym	false	false
351117014	Imerslund's syndrome	Active	Synonym	false	false

Associated Value Sets

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

Parent Concepts

Parent Concepts

Parent/Child (Relationship Type)

Autosomal recessive hereditary disorder (disorder) {85995004 , SNOMED-CT } Congenital anomaly of the hematopoietic system (disorder) {40888008 , SNOMED-CT } Disorder of sulfur-bearing amino acid metabolism (disorder) {28882002 , SNOMED-CT } Hemoglobin below reference range (finding) {165397008 , SNOMED-CT } Hereditary disorder of hematologic system (disorder) {363136009 , SNOMED-CT } Nutritional anemia (disorder) {66612000 , SNOMED-CT } Pernicious anemia (disorder) {84027009 , SNOMED-CT } Red blood cell count below reference range (finding) {165423001 , SNOMED-CT } Vitamin deficiency (disorder) {85670002 , SNOMED-CT }

Other Relationships

No other relationships present.

Child Concepts

No child concepts present.

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