Pages that link to "Property:P68"
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The following pages link to Canonical URI (P68):
Displaying 50 items.
- Acquired lymphocytosis (Q39648) (← links)
- Disorders with decreased monocyte counts (Q39649) (← links)
- Acquired decrease in eosinophil number (Q39650) (← links)
- Acquired disorders of neutrophil function (Q39651) (← links)
- Acquired neutrophilia (Q39652) (← links)
- Acquired lymphopenia (Q39653) (← links)
- Tumour-like conditions of spleen (Q39654) (← links)
- Acute septic splenitis (Q39655) (← links)
- Splenomegaly in storage diseases (Q39656) (← links)
- Infection of spleen (Q39657) (← links)
- Fibrosis of spleen (Q39658) (← links)
- Acquired disorders of spleen (Q39659) (← links)
- Postsurgical asplenia (Q39660) (← links)
- Splenosis (Q39661) (← links)
- Congenital disorders of spleen (Q39662) (← links)
- Torsion of spleen (Q39663) (← links)
- Perisplenitis (Q39664) (← links)
- Nontraumatic laceration or rupture of spleen (Q39665) (← links)
- Splenic cyst or pseudocyst (Q39666) (← links)
- Atrophy of spleen (Q39667) (← links)
- Hypersplenism (Q39668) (← links)
- Chronic congestive splenomegaly (Q39669) (← links)
- Abscess of spleen (Q39670) (← links)
- Epithelial cyst of spleen (Q39671) (← links)
- Pseudocyst of spleen (Q39672) (← links)
- Infarction of spleen (Q39673) (← links)
- Hereditary methaemoglobinaemia (Q39674) (← links)
- Congenital methaemoglobinaemia (Q39675) (← links)
- Acquired methaemoglobinaemia (Q39676) (← links)
- Primary inherited erythrocytosis (Q39677) (← links)
- Congenital polycythaemia (Q39678) (← links)
- Polycythaemia due to over-transfusion or blood doping (Q39679) (← links)
- Polycythaemia due to hypoxia, including high altitude (Q39680) (← links)
- Relative polycythaemia (Q39681) (← links)
- Acquired polycythaemia (Q39682) (← links)
- Reactive plasmacytic hyperplasia (Q39683) (← links)
- Primary haemophagocytic lymphohistiocytosis (Q39684) (← links)
- Diseases of immune dysregulation (Q39685) (← links)
- Juvenile xanthogranuloma (Q39686) (← links)
- Immune dysregulation syndromes presenting primarily with lymphoproliferation (Q39687) (← links)
- Histiocytoses of uncertain malignant potential (Q39688) (← links)
- Acquired fibrinolytic defects (Q39689) (← links)
- Hereditary agammaglobulinaemia with profoundly reduced or absent B cells (Q39690) (← links)
- Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells (Q39691) (← links)
- Immunodeficiencies with severe reduction in serum IgG or IgA with normal or elevated IgM and normal numbers of B-cells (Q39692) (← links)
- Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells (Q39693) (← links)
- Transient hypogammaglobulinaemia of infancy (Q39694) (← links)
- Immunodeficiencies with isotype or light chain deficiencies with normal number of B cells (Q39695) (← links)
- Immunodeficiencies with predominantly antibody defects (Q39696) (← links)
- Major histocompatibility complex class I deficiency (Q39697) (← links)
