D51.1
BillableVit B12 defic anemia d/t slctv vit B12 malabsorp w protein
Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Imerslund (Gräsbeck) syndrome
- Megaloblastic hereditary anemia
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- Megaloblastic anaemia due to vitamin B>12< malabsorption with proteinuria26333003
- Megaloblastic anemia due to vitamin B>12< malabsorption with proteinuria26333003
- Congenital pernicious anaemia34925000
- Congenital pernicious anemia34925000
- Megaloblastic anaemia due to inborn errors of metabolism34925000
- Megaloblastic anemia due to inborn errors of metabolism34925000
- Addison's anemia84027009
- Addisonian pernicious anaemia84027009
- Addisonian pernicious anemia84027009
- Biermer's anaemia84027009
- Biermer's anemia84027009
- Megaloblastic anaemia due to impaired absorption of cobalamin84027009
- Megaloblastic anemia due to impaired absorption of cobalamin84027009
- PA - Pernicious anaemia84027009
- Pernicious anaemia84027009
- Pernicious anemia84027009
- Vitamin B12 deficiency anaemia due to malabsorption with proteinuria191142007
- Vitamin B12 deficiency anemia due to malabsorption with proteinuria191142007
- Imerslund disease234363001
- Imerslund's syndrome234363001
- Imerslund-Grasbeck anaemia234363001
- Imerslund-Grasbeck anemia234363001
- Imerslund-Grasbeck disease234363001
- Imerslund-Grasbeck syndrome234363001
- Imerslund-Najman-Grasbeck syndrome234363001
- Selective malabsorption of cyanocobalamin234363001
- Vitamin B12 deficiency anaemia due to selective malabsorption of cyanocobalamin234363001
- Vitamin B12 deficiency anemia due to selective malabsorption of cyanocobalamin234363001
- Familial megaloblastic anaemia360495000
- Familial megaloblastic anemia360495000
UMLS
- Defect of enterocyte intrinsic factor receptorC4551825
- ENTEROCYTE COBALAMIN MALABSORPTIONC4551825
- ENTEROCYTE INTRINSIC FACTOR RECEPTOR, DEFECT OFC4551825
- Enterocyte cobalamin malabsorptionC4551825
- Enterocyte intrinsic factor receptor, defect ofC4551825
- IGS1C4551825
- IMERSLUND-GRASBECK SYNDROME 1C4551825
- Imerslund (Gräsbeck) syndromeC4551825
- Imerslund diseaseC4551825
- Imerslund's syndromeC4551825
- Imerslund-Graesbeck syndromeC4551825
- Imerslund-Grasbeck anaemiaC4551825
- Imerslund-Grasbeck anemiaC4551825
- Imerslund-Grasbeck diseaseC4551825
- Imerslund-Grasbeck syndromeC4551825
- Imerslund-Gräsbeck syndromeC4551825
- Imerslund-Najman-Grasbeck syndromeC4551825
- Juvenile pernicious anemia with proteinuria due to selective intestinal malabsorption of vitamin B12C4551825
- MEGALOBLASTIC ANEMIA, 1C4551825
- MGA1C4551825
- Megaloblastic Anemia 1C4551825
- Megaloblastic anemia 1C4551825
- PERNICIOUS ANEMIA, JUVENILE, DUE TO SELECTIVE INTESTINAL MALABSORPTION OF VITAMIN B12, WITH PROTEINURIAC4551825
- Selective malabsorption of cyanocobalaminC4551825
- Selective malabsorption of cyanocobalamin (disorder)C4551825
- Vitamin B12 deficiency anaemia due to selective malabsorption of cyanocobalaminC4551825
- Vitamin B12 deficiency anemia due to selective malabsorption of cyanocobalaminC4551825
- Megaloblastic hereditary anemiaC1387565
- Vit B12 defic anemia d/t slctv vit B12 malabsorp w proteinC0494218
- Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuriaC0494218
Frequently Asked Questions
What is ICD-10 code D51.1?
ICD-10-CM code D51.1 represents "Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria". It is a billable/specific code that can be used on a claim.
Is D51.1 a billable code?
Yes, D51.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D51.1 in?
D51.1 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D51.1?
D51.1 has Excludes1 notes indicating codes that cannot be used together with it, including: vitamin B12 deficiency (E53.8).
What SNOMED CT codes does D51.1 map to?
D51.1 maps to 6 SNOMED CT concepts: 84027009, 34925000, 360495000, 234363001, 26333003, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D51.1?
D51.1 is linked to 3 UMLS Concept Unique Identifiers: C4551825, C1387565, C0494218. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.