D51.0
BillableVitamin B12 defic anemia due to intrinsic factor deficiency
Vitamin B12 deficiency anemia due to intrinsic factor deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Addison anemia
- Biermer anemia
- Pernicious (congenital) anemia
- Congenital intrinsic factor deficiency
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
- Congenital pernicious anaemia34925000
- Congenital pernicious anemia34925000
- Megaloblastic anaemia due to inborn errors of metabolism34925000
- Megaloblastic anemia due to inborn errors of metabolism34925000
- Congenital intrinsic factor deficiency anaemia60504009
- Congenital intrinsic factor deficiency anemia60504009
- Megaloblastic anaemia due to congenital deficiency of intrinsic factor60504009
- Megaloblastic anemia due to congenital deficiency of intrinsic factor60504009
- 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
- Myasthenic syndrome due to another disorder193209005
- Myasthenic syndrome due to pernicious anaemia193213003
- Myasthenic syndrome due to pernicious anemia193213003
- Congenital deficiency of intrinsic factor234361004
- Biermer congenital pernicious anaemia234362006
- Biermer congenital pernicious anemia234362006
- Biermer's congenital pernicious anaemia234362006
- Biermer's congenital pernicious anemia234362006
- Pernicious anaemia due to autoimmune disorder1153333001
- Pernicious anemia due to autoimmune disorder1153333001
UMLS
- Addison AnemiaC0002892
- Addison anemiaC0002892
- Addison's AnemiaC0002892
- Addison's anaemiaC0002892
- Addison's anemiaC0002892
- Addison-Biermer anaemiaC0002892
- Addison-Biermer anemiaC0002892
- Addisonian anaemiaC0002892
- Addisonian anemiaC0002892
- Addisonian pernicious anaemiaC0002892
- Addisonian pernicious anemiaC0002892
- Addisons AnemiaC0002892
- Anaemia perniciousC0002892
- Anaemia pernicious typeC0002892
- Anemia pernicious typeC0002892
- Anemia, AddisonC0002892
- Anemia, Addison'sC0002892
- Anemia, AddisonsC0002892
- Anemia, PerniciousC0002892
- Biermer anemiaC0002892
- Biermer's anaemiaC0002892
- Biermer's anemiaC0002892
- Megaloblastic anaemia due to impaired absorption of cobalaminC0002892
- Megaloblastic anemia due to impaired absorption of cobalaminC0002892
- PA - Pernicious anaemiaC0002892
- PERNICIOUS ANEMIAC0002892
- Pernicious AnemiaC0002892
- Pernicious anaemiaC0002892
- Pernicious anaemia NOSC0002892
- Pernicious anemiaC0002892
- Pernicious anemia (disorder)C0002892
- addison's anemiaC0002892
- addison-biermer anemiaC0002892
- addisonian anemiaC0002892
- pernicious anaemiaC0002892
- pernicious anemiaC0002892
- Congenital deficiency of intrinsic factorC2062370
- Congenital deficiency of intrinsic factor (disorder)C2062370
- Congenital intrinsic factor deficiencyC2062370
- IFDC2062370
- INTRINSIC FACTOR DEFICIENCYC2062370
- Intrinsic Factor DeficiencyC2062370
- PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTORC2062370
- Pernicious Anemia, Congenital, due to Defect of Intrinsic FactorC2062370
- Congenital pernicious anaemiaC1306856
- Congenital pernicious anemiaC1306856
- Familial megaloblastic anaemiaC1306856
- Familial megaloblastic anemiaC1306856
- Familial megaloblastic anemia (disorder)C1306856
- Juvenile type megaloblastic anaemiaC1306856
- Juvenile type megaloblastic anemiaC1306856
- Juvenile type megaloblastic anemia (disorder)C1306856
- Megaloblastic anaemia due to inborn errors of metabolismC1306856
- Megaloblastic anemia due to inborn errors of metabolismC1306856
- Megaloblastic anemia due to inborn errors of metabolism (disorder)C1306856
- Pernicious (congenital) anemiaC1306856
- Vitamin B12 defic anemia due to intrinsic factor deficiencyC0494217
- Vitamin B12 deficiency anemia due to intrinsic factor deficiencyC0494217
Frequently Asked Questions
What is ICD-10 code D51.0?
ICD-10-CM code D51.0 represents "Vitamin B12 deficiency anemia due to intrinsic factor deficiency". It is a billable/specific code that can be used on a claim.
Is D51.0 a billable code?
Yes, D51.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D51.0 in?
D51.0 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D51.0?
D51.0 has Excludes1 notes indicating codes that cannot be used together with it, including: vitamin B12 deficiency (E53.8).
What SNOMED CT codes does D51.0 map to?
D51.0 maps to 8 SNOMED CT concepts: 84027009, 234362006, 234361004, 60504009, 34925000, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D51.0?
D51.0 is linked to 4 UMLS Concept Unique Identifiers: C0002892, C2062370, C1306856, C0494217. 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.