Pages that link to "Property:P89"
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The following pages link to Linked ICD 10 (P89):
Displaying 50 items.
- 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)
- Sarcoidosis of the digestive system (Q39722) (← links)
- Neurosarcoidosis (Q39723) (← links)
- Sarcoidosis (Q39724) (← links)
- Polyclonal hypergammaglobulinaemia (Q39725) (← links)
- Cryoglobulinaemia (Q39726) (← links)
- Cryoglobulinaemic vasculitis (Q39727) (← links)
- Immune reconstitution inflammatory syndrome (Q39729) (← links)
- Tumour necrosis factor receptor 1 associated periodic syndrome (Q39730) (← links)
- Familial Mediterranean fever (Q39731) (← links)
- Cryopyrin-associated periodic syndromes (Q39732) (← links)
- Immune dysregulation syndromes presenting primarily with autoimmunity (Q39733) (← links)
- Hepatic veno-occlusive disease - immunodeficiency syndrome (Q39734) (← links)
- Immune dysregulation syndromes with hypopigmentation (Q39735) (← links)
- Neutrophilia (Q39736) (← links)
- Adult-onset immunodeficiency (Q39737) (← links)
- Acquired immunodeficiencies (Q39738) (← links)
- Disorders of neutrophil number (Q39739) (← links)
