anemia
Basic Information
- Identifier
- SYMP_0000208
- Notation
- SYMP:0000208
- Category
- symptoms
- Synonyms
-
- anaemia
Related Diseases
- 3-methylglutaconic aciduria type 5
- AMED syndrome
- B acute lymphoblastic leukemia with DUX4 rearrangement
- B-cell acute lymphoblastic leukemia
- B-lymphoblastic leukemia/lymphoma with BCR-ABL1
- B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1
- B-lymphoblastic leukemia/lymphoma with IL3-IGH
- B-lymphoblastic leukemia/lymphoma with hypodiploidy
- B-lymphoblastic leukemia/lymphoma with iAMP21
- B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like
- Carrion's disease
- Chanarin-Dorfman syndrome
- Crohn's disease
- Diamond-Blackfan anemia 15 with mandibulofacial dysostosis
- Fanconi anemia complementation group I
- Fanconi anemia complementation group L
- Fanconi anemia complementation group O
- Fanconi anemia complementation group V
- Pearson syndrome
- Rh deficiency syndrome
- Rh isoimmunization
- SM-AHNMD
- Schimke immuno-osseous dysplasia
- Shwachman-Diamond syndrome
- Stormorken syndrome
- T-cell childhood lymphoblastic lymphoma
- T-cell large granular lymphocyte leukemia
- TFE3-rearranged renal cell carcinoma
- TORCH syndrome
- Whipple disease
- Wolman disease
- X-linked thrombocytopenia with beta-thalassemia
- abetalipoproteinemia
- acquired thrombocytopenia
- acute myeloid leukemia with BCR-ABL1
- acute myeloid leukemia with biallelic mutation of CEBPA
- acute myeloid leukemia with minimal differentiation
- acute myeloid leukemia with mutated NPM1
- acute myeloid leukemia with t(1;22)(p13;q13)
- acute myeloid leukemia with t(6;9) (p23;q34.1)
- acute myeloid leukemia without maturation
- adenosarcoma
- aleutian mink disease
- alpha thalassemia-X-linked intellectual disability syndrome
- alpha-thalassemia myelodysplasia syndrome
- alveolar echinococcosis
- ancylostomiasis
- angiodysplasia
- atypical chronic myeloid leukemia, BCR-ABL1 negative
- autosomal genetic disease
- autosomal recessive dyskeratosis congenita 2
- autosomal recessive osteopetrosis 2
- autosomal recessive osteopetrosis 4
- autosomal recessive osteopetrosis 5
- autosomal recessive osteopetrosis 7
- autosomal recessive pyridoxine-refractory sideroblastic anemia 2
- babesiosis
- beta-thalassemia major
- cecal benign neoplasm
- cecum adenoma
- childhood acute lymphocytic leukemia
- childhood acute myeloid leukemia
- childhood renal cell carcinoma with MiT translocations
- chorioangioma
- chromosome 15q25 deletion syndrome
- chromosome 5q deletion syndrome
- chronic congestive splenomegaly
- chronic lymphocytic leukemia
- chronic lymphocytic leukemia/small lymphocytic lymphoma
- chronic neutrophilic leukemia
- colorectal adenoma
- congenital disorder of glycosylation Iq
- congenital dyserythropoietic anemia
- congenital dyserythropoietic anemia type I
- congenital dyserythropoietic anemia type II
- copper deficiency myelopathy
- delta chain disease
- dialysis-related amyloidosis
- disease of cellular proliferation
- endometrial adenosquamous carcinoma
- endometrium carcinoma in situ
- eosinophilic variant of chromophobe renal cell carcinoma
- esophageal varix
- familial adenomatous polyposis
- familial adenomatous polyposis 4
- fascioloidiasis
- fibrodysplasia ossificans progressiva
- gallbladder angiosarcoma
- gamma heavy chain disease
- gastric antral vascular ectasia
- gastrointestinal system benign neoplasm
- glycoproteinosis
- hemangioma of liver
- hepatosplenic T-cell lymphoma
- hereditary folate malabsorption
- hereditary spherocytosis
- hereditary spherocytosis type 3
- hereditary spherocytosis type 4
- hereditary spherocytosis type 5
- homocystinuria-megaloblastic anemia cblE type
- homocystinuria-megaloblastic anemia cblG type
- human cytomegalovirus infection
- hypersplenism
- hypogonadism
- hypogonadotropic hypogonadism 6 with or without anosmia
- hypogonadotropic hypogonadism 9 with or without anosmia
- immunodeficiency 14
- immunodeficiency 32B
- infantile liver failure syndrome 1
- jejunal neoplasm
- juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
- juvenile xanthogranuloma
- kidney cortex disease
- kidney lipoma
- lymphoproliferative syndrome
- lymphoproliferative syndrome 2
- malignant adenoma
- malignant fibrous histiocytoma
- malignant histiocytic disease
- malignant inflammatory fibrous histiocytoma
- malignant neoplasm of short bones of lower limb
- mast cell neoplasm
- methylmalonic acidemia cblB type
- methylmalonic aciduria and homocystinuria type cblD
- methylmalonic aciduria and homocystinuria type cblF
- methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
- mitochondrial complex III deficiency nuclear type 4
- mitochondrial complex IV deficiency nuclear type 1
- mitochondrial complex IV deficiency nuclear type 13
- mitochondrial complex IV deficiency nuclear type 3
- mitochondrial complex IV deficiency nuclear type 4
- mitochondrial complex IV deficiency nuclear type 7
- mixed phenotype acute leukemia, T/myeloid
- mu chain disease
- mucocele of appendix
- myeloid and lymphoid neoplasms associated with PDGFRA rearrangement
- myeloid and lymphoid neoplasms associated with PDGFRB rearrangement
- myelophthisic anemia
- myeloproliferative disorder with eosinophilia
- myopathy, lactic acidosis, and sideroblastic anemia
- myopathy, lactic acidosis, and sideroblastic anemia 1
- myopathy, lactic acidosis, and sideroblastic anemia 2
- myopathy, lactic acidosis, and sideroblastic anemia 3
- necatoriasis
- nephronophthisis 1
- nephronophthisis 11
- nephronophthisis 12
- nephronophthisis 13
- nephronophthisis 16
- nephronophthisis 18
- nephronophthisis 2
- nephronophthisis 3
- nephronophthisis 7
- nephronophthisis 9
- nuclear type mitochondrial complex I deficiency 4
- obsolete Ancylostoma braziliense ancylostomiasis
- obsolete Ancylostoma caninum ancylostomiasis
- obsolete Anelloviridae infectious disease
- obsolete HIV enteropathy
- obsolete Parvoviridae infectious disease
- obsolete agalactia
- obsolete bovine anaplasmosis
- obsolete bovine trypanosomiasis
- obsolete chronic glomerulonephritis with lesion of membranous glomerulonephritis
- obsolete chronic glomerulonephritis with lesion of proliferative glomerulonephritis
- obsolete equine infectious anemia
- obsolete gastric mesenchymal neoplasm
- obsolete hairy cell leukemia of spleen
- obsolete intestinal strongyloidiasis
- obsolete lymphoma by site
- obsolete megakaryocytic tumor
- obsolete metastasis to prostate
- obsolete myeloid metaplasia
- obsolete opportunistic ascomycota mycosis
- obsolete paraproteinemia
- obsolete peripheral dysostosis
- obsolete recurrent renal cell carcinoma
- obsolete recurrent stomach cancer
- obsolete secondary malignant neoplasm to the thymus
- obsolete spleen mast cell malignancy
- obsolete sporadic conventional renal cell carcinoma
- obsolete ssDNA virus infectious disease
- orotic aciduria
- pancreatic somatostatinoma
- penicilliosis
- proteasome-associated autoinflammatory syndrome 3
- purpura fulminans
- renal adenoma
- renal cell carcinoma
- reticular dysgenesis
- retroperitoneal cancer
- riboflavin deficiency
- scurvy
- sialuria
- sickle cell disease
- sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay
- signet ring basal cell carcinoma
- small intestine lymphoma
- soft tissue peripheral neuroepithelioma
- submucosal invasive colon adenocarcinoma
- systemic mastocytosis
- thalassemia
- theileriasis
- thiamine-responsive megaloblastic anemia syndrome
- toxoplasmosis
- transcobalamin II deficiency
- transient infantile liver failure
- trichostrongylosis
- trichuriasis
- tropical sprue
- vitamin metabolic disorder
- warfarin resistance
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