Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
Billable / specific
D51.1 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Imerslund (Gräsbeck) syndrome
- Megaloblastic hereditary anemia
Excludes2
Not included here — may be reported together when both conditions exist.
- autoimmune disease (systemic) NOS (M35.9) (from D51)
- certain conditions originating in the perinatal period (P00-P96) (from D51)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D51)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D51)
- endocrine, nutritional and metabolic diseases (E00-E88) (from D51)
- human immunodeficiency virus [HIV] disease (B20) (from D51)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from D51)
- neoplasms (C00-D49) (from D51)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D51)
- deficiency of other B group vitamins (E53-) (from D51)
Also known as
- Imerslund (Gräsbeck) syndrome
- Megaloblastic hereditary anemia
- Anemia, due to selective vitamin B12 malabsorption with proteinuria
- Anemia, megaloblastic, hereditary
- Imerslundsyndrome
Parent code
- D51Vitamin B12 deficiency anemiaHeader