D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
Billable ICD-10-CM code, FY2026.
Applicable to
- Addison anemia
- Biermer anemia
- Pernicious (congenital) anemia
- Congenital intrinsic factor deficiency
Applies from D51 Vitamin B12 deficiency anemia
Excludes1 (never code together)
- vitamin B12 deficiency (E53.8)
MS-DRG index
Defines the logic of DRG(s) 811-812 in MDC 16.
Approximate ICD-9-CM (GEMs)
281.0 Pernicious anemia (approximate)
Code annotations containing back-references to D51.0
Back-references to D51.0
- Code First:
G32.0 Subacute combined degeneration of spinal cord in diseases classified elsewhere ("vitamin B12 deficiency anemia due to intrinsic factor deficiency (D51.0)")
Back-references to D51
- Type 1 Excludes:
E53.8 Deficiency of other specified B group vitamins ("vitamin B12 deficiency anemia (D51.-)") - Code First:
M90.5 Osteonecrosis in diseases classified elsewhere ("hemoglobinopathy (D50-D64)") - Type 1 Excludes:
R71 Abnormality of red blood cells ("anemias (D50-D64)")
Diagnosis Index entries for D51.0
- Addison's › anemia (pernicious)
- Addison-Biermer anemia (pernicious)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › Addison (-Biermer) (pernicious)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › Biermer's (pernicious)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › combined system disease NEC
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › congenital › pernicious
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › cytogenic
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › deficiency › vitamin B12 NOS › due to › intrinsic factor deficiency
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › deficiency › vitamin B12 NOS › pernicious
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › malignant (progressive)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › pernicious (congenital) (malignant) (progressive)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › progressive › malignant
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › progressive › pernicious
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › vitamin › B12 deficiency (dietary) pernicious
- Biermer's (pernicious) anemia or disease
- Congenital › intrinsic factor deficiency
- Deficiency, deficient › intrinsic › factor (congenital)
- Degeneration, degenerative › combined (spinal cord) (subacute) › with anemia (pernicious)
- Disease, diseased › Addison's anemia (pernicious)
- Disease, diseased › Biermer's (pernicious anemia)
- Disease, diseased › Lichtheim's (subacute combined sclerosis with pernicious anemia)
- Disease, diseased › Putnam's (subacute combined sclerosis with pernicious anemia)
- Disease, diseased › Runeberg's (progressive pernicious anemia)
- Glossitis (chronic superficial) (gangrenous) (Moeller's) › Hunter's
- Hunter's › glossitis
- Lichtheim's disease or syndrome
- Myasthenia › syndrome › in › pernicious anemia
- Myelopathy (spinal cord) › in (due to) › pernicious anemia
- Neuropathy, neuropathic › vitamin B12 › with anemia (pernicious)
- Polyneuropathy (peripheral) › in (due to) › vitamin B12 deficiency › with anemia (pernicious)
- Runeberg's disease
- Syndrome › Dana-Putnam
- Syndrome › hunterian glossitis
- Syndrome › Lichtheim's
- Syndrome › Putnam-Dana
Nearby codes
D51 Vitamin B12 deficiency anemiaD51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency (this code)D51.1 Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuriaD51.2 Transcobalamin II deficiencyD51.3 Other dietary vitamin B12 deficiency anemiaD51.8 Other vitamin B12 deficiency anemiasD51.9 Vitamin B12 deficiency anemia, unspecified