| Disease Browser
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Parent Node:
 Hematologic Diseases (D006402) |
..Starting node
.. Leukocyte Disorders (D007960)
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Child Nodes:
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| ........Cd4+ Lymphocyte Deficiency (C566079) |
........Eosinophilia (D004802)  18 |
| ........Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis (C564365) |
| ........Infectious Mononucleosis (D007244) |
| ........Lazy Leukocyte Syndrome (C562721) |
| ........Leukocyte Nuclear Appendages, Hereditary Prevalence of (C563626) |
| ........Leukocytosis (D007964) 6 |
| ........Leukopenia (D007970) 27 |
| ........Leukostasis (D018921) |
| ........Monocyte Esterase Deficiency (C566173) |
| ........Neutrophil Actin Dysfunction (C564942) |
| ........Neutrophil Chemotactic Response, Abnormal (C563515) |
| ........Neutrophilia, Hereditary (C563010) |
| ........Pelger-Huet Anomaly (D010381) |
| ........Pelger-Huet-Like Anomaly and Episodic Fever with Abdominal Pain (C564899) |
| ........Phagocyte Bactericidal Dysfunction (D010585) 14 |
| ........Phagocytosis, Plasma-Related Defect in (C566808) |
| ........Presentey Anomaly (C564893) |
| ........Specific Granule Deficiency (C562873) |
| ........T-Cell OKT4 Deficiency (C566080) |
| ........Undritz Anomaly (C566014) |
Sister Nodes: |
..Adenosine Triphosphate, Elevated, Of Erythrocytes (C566310)
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..Anemia (D000740) 166
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..Blood Coagulation Disorders (D001778) 119
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..Blood Platelet Disorders (D001791) 93
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..Blood Protein Disorders (D001796) 75
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..Bone Marrow Diseases (D001855) 87
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..Erythroblastosis, Fetal (D004899) 7
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..Hematologic Neoplasms (D019337) 1
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..Hemoglobinopathies (D006453) 23
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..Hemorrhagic Disorders (D006474) 108
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..Kabuki syndrome (C537705)
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..Leukocyte Disorders (D007960) 84
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..Macrocytosis, Familial (C564004)
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..Methemoglobinemia (D008708) 6
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..Pancytopenia (D010198) 5
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..Polycythemia (D011086) 4
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..Pregnancy Complications, Hematologic (D011250)
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..Preleukemia (D011289)
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..Rh-Null, Regulator Type (C564833)
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..Sulfhemoglobinemia (D013436) 1
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..Thrombophilia (D019851) 27
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..Transfusion Reaction (D065227)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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