Pages that link to "Property:P78"
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The following pages link to Knowledge Architect (P78):
Displaying 50 items.
- 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)
- Major histocompatibility complex class II deficiency (Q39698) (← links)
- Severe combined immunodeficiencies (Q39699) (← links)
- Combined immunodeficiencies (Q39700) (← links)
- CATCH 22 phenotype (Q39701) (← links)
- Hyperimmunoglobulin E syndromes (Q39702) (← links)
- Hereditary angioedema (Q39703) (← links)
- Immunodeficiency with a late component of complement deficiency (Q39704) (← links)
- Immunodeficiency with an early component of complement deficiency (Q39705) (← links)
- Defects in the complement system (Q39706) (← links)
- Immunodeficiency with factor B deficiency (Q39707) (← links)
- Immunodeficiency with factor D anomaly (Q39708) (← links)
- Acquired angioedema (Q39709) (← links)
- Genetic susceptibility to particular pathogens (Q39710) (← links)
- Immunodeficiency with natural-killer cell deficiency (Q39711) (← links)
- Immunodeficiency due to defects of the thymus (Q39712) (← links)
- Primary immunodeficiencies due to disorders of adaptive immunity (Q39713) (← links)
- Other well-defined immunodeficiency syndromes due to defects in adaptive immunity (Q39714) (← links)
- Immuno-osseous dysplasia (Q39715) (← links)
- DNA repair defects other than combined T-cell or B-cell immunodeficiencies (Q39716) (← links)
- Primary immunodeficiencies due to disorders of innate immunity (Q39717) (← links)
- Sarcoidosis of lung (Q39718) (← links)
- Sarcoidosis of lymph nodes (Q39719) (← links)
- Cutaneous sarcoidosis (Q39720) (← links)
- Ocular sarcoidosis (Q39721) (← links)
