Human (102 sources):
Abdominal pain,
Abnormal bleeding,
Abnormal bone marrow cell morphology,
Abnormal cardiac ventricular function,
Abnormal circulating albumin concentration,
Abnormal circulating protein concentration,
Abnormal fingernail morphology,
Abnormality of blood and blood-forming tissues,
Abnormal mean corpuscular volume,
Abnormal megakaryocyte morphology,
Abnormal number of granulocyte precursors,
Abnormal thrombosis,
Acute leukemia,
Acute myeloid leukemia,
Anemia,
Anemia of inadequate production,
Anemic pallor,
Angina pectoris,
Anorexia,
Arterial thrombosis,
Arthralgia,
Bone marrow hypercellularity,
Bone marrow hypocellularity,
Bone pain,
Bruising susceptibility,
Budd-Chiari syndrome,
Cachexia,
Cerebral hemorrhage,
Cerebral ischemia,
Chronic infection,
Chronic myelogenous leukemia,
Chronic myelomonocytic leukemia,
Congestive heart failure,
Constitutional symptom,
Decreased total granulocyte count,
Decreased total neutrophil count,
Dysplastic granulopoesis,
Dyspnea,
Easy fatigability,
Ecchymosis,
Epistaxis,
Erythroid hyperplasia,
Erythroid hypoplasia,
Exertional dyspnea,
Extramedullary hematopoiesis,
Fatigue,
Fever,
Flank pain,
Gastrointestinal hemorrhage,
Gingival bleeding,
Headache,
Hemangioma,
Hematological neoplasm,
Hepatomegaly,
Hepatosplenomegaly,
Hypertension,
Hypochromic anemia,
Hyposegmentation of neutrophil nuclei,
Increased circulating hemoglobin concentration,
Increased circulating lactate dehydrogenase concentration,
Increased hematocrit,
Increased megakaryocyte count,
Increased red blood cell mass,
Increased total eosinophil count,
Increased total leukocyte count,
Intermittent claudication,
Low-grade fever,
Lymphadenopathy,
Macrocytic anemia,
Mastocytosis,
Megaloblastic erythroid hyperplasia,
Multiple lineage myelodysplasia,
Myelodysplasia,
Myelofibrosis,
Myeloproliferative disorder,
Non-Hodgkin lymphoma,
Normochromic anemia,
Normocytic anemia,
Pallor,
Palpitations,
Pancytopenia,
Pedal edema,
Petechiae,
Poikilocytosis,
Portal hypertension,
Portal vein thrombosis,
Pruritus,
Pulmonary embolism,
Purpura,
Refractory anemia with ringed sideroblasts,
Respiratory insufficiency,
Retinal hemorrhage,
Single lineage myelodysplasia,
Splenomegaly,
Stroke,
Thrombocytopenia,
Thrombocytosis,
Thromboembolism,
Tinnitus,
Venous thrombosis,
Vertigo,
Weight loss
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Gene expression phenotype annotations where the gene of interest has been
disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from
differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1,
FDR <= 0.05 and an absolute LogFC >= 2.