This likely indicates inadequate absorption
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We merged genes from the three databases to create a gene set for each pathway (Additional file 1: Tables S2S4), resulting in 5325, 2557, and 3435 genes for Most Studied Pathways, Gene-Associated Pathways, and Popular Pathways, respectively
- Dana-Putnam - D51.0 - hunterian glossitis - D51.0 - Lichtheim's - D51.0 - Putnam-Dana - D51.0 Index of External Cause of Injuries References found for this diagnosis code in the External Cause of Injuries Index: 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 Convert D51.0 to ICD-9-CM Below are the ICD-9 codes that most closely match this ICD-10 code, based on the General Equivalence Mappings (GEMs)
