Alphabetical Index of Conditions

Condition
Acquired coagulation factor inhibitors (alloantibodies and autoantibodies), including acquired haemophilia, acquired von Willebrand syndrome, inhibitors to FVIII in haemophilia A, and inhibitors to FIx in haemophilia B (see coagulation factor inhibitors)
Acquired hypogammaglobulinaemia secondary to haematological malignancies (chronic lymphocytic leukaemia, multiple myeloma, non-Hodgkin lymphoma, and other relevant malignancies and post-haemopoietic stem cell transplantation)
Acute autonomic neuropathy (see guillain–Barré syndrome)
Acute disseminated encephalomyelitis
Acute inflammatory demyelinating polyneuropathy (see guillain–Barré syndrome)
Acute leukaemia in children
Acute motor axonal neuropathy (see guillain–Barré syndrome)
Acute motor sensory axonal neuropathy (see guillain–Barré syndrome)
Acute optic neuritis
Acute rheumatic fever
Adrenoleukodystrophy
Amegakaryocytic thrombocytopenia
Amyotrophic lateral sclerosis (see motor neuron disease)
ANCA-positive systemic necrotising vasculitis
Antiphospholipid syndrome — non-obstetric
Aplastic anaemia/pancytopenia
Asthma
Atopic dermatitis/eczema (adult)
Autism
Autoimmune congenital heart block (neonatal lupus)
Autoimmune haemolytic anaemia
Autoimmune haemolytic anaemia with immune thrombocytopenia (see Evans syndrome)
Autoimmune neutropenia
Autoimmune uveitis
Autologous haemopoietic stem cell transplantation
Behçet’s disease
Bickerstaff’s brainstem encephalitis (see guillain–Barré syndrome)
Bullous pemphigoid
Capillary leak syndrome (see Systemic capillary leak syndrome)
Cardiac failure — congestive
Cardiac surgery with bypass — prophylaxis
Cataplexy (see narcolepsy)
Catastrophic antiphospholipid syndrome
Chronic inflammatory demyelinating polyneuropathy (CIDP)
Cicatricial pemphigoid
Coagulation factor inhibitors (alloantibodies and autoantibodies) — including acquired haemophilia, acquired von Willebrand syndrome, inhibitors to FVIII in haemophilia A, and inhibitors to FIX in haemophilia B
Common variable immunodeficiency (CVID) (see primary immunodeficiency)
Congenital heart block (see autoimmune congenital heart block)
Congestive cardiac failure
Crohn’s disease
Dermatitis/eczema atopic (adult) (see atopic dermatitis/eczema)
Demyelinating polyneuropathy (see chronic inflammatory)
Dermatomyositis (see inflammatory myopathies)
Devic disease (neuromyelitis optica)
Diabetic amyotrophy
Diabetic lumbosacral radiculoplexus neuropathy (see diabetic amyotrophy)
Diabetic proximal neuropathy (see diabetic amyotrophy)
Diamond Blackfan syndrome
Eczema, atopic dermatitis (adult) (see atopic dermatitis/eczema)
Encephalomyelitis - acute disseminated (see acute disseminated)
Encephalopathy (see Hashimoto)
Encephalopathy (see limbic - nonparaneoplastic)
Encephalopathy (see limbic - paraneoplastic)
Encephalopathy (see potassium channel)
Epidermolysis bullosa acquisita
Epilepsy - rare childhood cases
Evans syndrome - autoimmune haemolytic anaemia with immune thrombocytopenia
Female infertility
Foeto-maternal/neonatal alloimmune thrombocytopenia (FMAIT/NAIT)
Glomerulonephritis – IgA nephritis
Graves ophthalmopathy
Guillain–Barré syndrome (gBS)
Haemolytic anaemia (see autoimmune haemolytic anaemia)
Haemolytic anaemia — autoimmune with immune thrombocytopenia (see Evans syndrome)
Haemolytic disease of the newborn
Haemolytic transfusion reaction
Haemolytic uraemic syndrome
Haemophagocytic syndrome
Haemopoietic stem cell transplant (see autologous)
Hashimoto encephalopathy
Heart block (see autoimmune congenital)
Henoch–Schonlein purpura
HIV/AIDS — adult
HIV/AIDS — children
Iatrogenic immunodeficiency (see secondary hypogammaglobulinaemia)
Idiopathic dilated cardiomyopathy
Idiopathic thrombocytopenic purpura (ITP) — adults
Idiopathic thrombocytopenic purpura (ITP) — child
IgA nephritis (see glomerulonephritis)
IgG subclass deficiency (see specific antibody deficiency)
IgM paraproteinaemic neuropathy
Inclusion body myositis (see inflammatory myopathies)
Inflammatory myopathies (polymyositis, dermatomyositis, inclusion body myositis)
Inhibitors — coagulation factor (alloantibodies and autoantibodies), including acquired haemophilia, acquired von Willebrand syndrome, inhibitors to FVIII in haemophilia A, and inhibitors to FIx in haemophilia B (see coagulation factor inhibitors)
Kawasaki disease
Kidney transplantation
Lambert–Eaton myasthenic syndrome
Landau–Keffner syndrome (see Epilepsy)
Lennox–gastaut syndrome (see Epilepsy)
Leukaemia in children (see acute leukaemia in children)
Lewis-Sumner syndrome variant (see Guillain–Barré syndrome)
Limbic encephalitis, nonparaneoplastic
Limbic encephalitis, paraneoplastic
Linear IgA disease
Lupus cerebritis
Lupus nephritis
Lyell syndrome (see Toxic epidermal necrolysis)
Miller Fisher syndrome (see Guillain–Barré syndrome)
Moersch-Woltman syndrome (see Stiff person syndrome)
Motor neuron disease/amyotrophic lateral sclerosis
Mucocutaneous lymph node syndrome (see Kawasaki Disease)
Mucous membrane pemphigoid (see cicatricial pemphigoid)
Multifocal motor neuropathy
Multiple sclerosis
Myalgic encephalomyelitis
Myasthenia gravis
Myocarditis in children
Narcolepsy/cataplexy
Neonatal alloimmune thrombocytopenia (NAIT) (see Foeto - maternal)
Neonatal haemochromatosis
Neonatal lupus (see autoimmune congenital heart block)
Nephrotic syndrome
Neuromyelitis optica (see Devic disease)
Neuropathy (see Chronic inflammatory demyelinating)
Neuropathy (see diabetic amyotrophy)
Neuropathy (see IgM paraproteinaemic)
Neuropathy (see multifocal motor)
Neuropathy (see paraneoplastic subacute sensory)
Neuropathy (see polyneuropathy of critical illness)
Neutropenia (see autoimmune neutropenia)
Obsessive compulsive disorders
Opsoclonus-myoclonus ataxia
Optic neuritis (see acute optic neuritis)
Paediatric autoimmune neuropsychiatric disorder associated with streptococcal infections (PANDAS)
Pancytopenia (see aplastic anaemia)
Paraneoplastic cerebellar degeneration
Paraneoplastic limbic encephalitis (see limbic encephalitis – paraneoplastic)
Paraneoplastic neurological syndromes (see paraneoplastic subacute sensory neuropathy, Paraneoplastic cerebellar degeneration, limbic encephalitis paraneoplastic)
Paraneoplastic subacute sensory neuropathy
Pemphigus foliaceus
Pemphigus vulgaris
Polymyositis (see inflammatory myopathies)
Polyneuropathy of critical illness
Post-transfusion purpura
Potassium channel antibody-associated encephalopathy
Primary immunodeficiency diseases with antibody deficiency
Pure red cell aplasia
Pure white cell aplasia
Pyoderma gangrenosum
Rasmussen syndrome
Recurrent foetal loss (with or without antiphospholipid syndrome)
Renal transplantation (see kidney transplantation)
Rheumatic fever (see acute rheumatic fever)
Rheumatoid arthritis
Scleromyxedema
Secondary hypogammaglobulinaemia (including iatrogenic immunodeficiency)
Sepsis
Sickle cell disease
Sjogren’s syndrome
Solid organ transplantation (other than kidney)
Specific antibody deficiency
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (see Hashimoto)
Stevens–Johnson syndrome (see toxic epidermal necrolysis/SJS)
Stiff person syndrome
Susac syndrome
Systemic capillary leak syndrome
Systemic lupus erythematosus (SLE)
Systemic necrotising vasculitis (see ANCA-positive systemic necrotising vasculitis)
Thrombocytopenia (see amegakaryocytic)
Thrombocytopenia (see Evans syndrome)
Thrombocytopenia (see idiopathic thrombocytopenia purpura)
Thrombocytopenia (see neonatal alloimmune thrombocytopenia)
Thrombocytopenia (see post-transfusion purpura)
Transient hypogammaglobulinaemia of infancy (see primary immunodeficiency disease)
Toxic epidermal necrolysis/Stevens–Johnson syndrome (TEN/SJS)
Toxic shock syndrome
Ulcerative colitis
Uveitis (see autoimmune uveitis)
Wiskott–Aldrich syndrome (see primary immunodeficiency disease)
X-linked agammaglobulinaemia (see primary immunodeficiency disease)