Disease Index
9,486 diseasesautoimmune hypophysitis
inflammation of the pituitary gland due to autoimmunity
MeSH: D000069281
autoimmune lymphoproliferative syndrome
Human disease
MeSH: D056735
autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency
somatic mutation in the CTLA4 gene resulting in only a single functional gene. Haploinsufficiency for CTLA4 is associated with autoimmune lymphoproliferative syndrome, type V
autoimmune pancreatitis
type of chronic pancreatitis
MeSH: D000081012
autoimmune pancreatitis type 1
60 years) and presenting with abdominal pain, steatorrhea, obstructive jaundice and other organ (bile duct, kidneys and retroperitoneum) involvement. It is thought to be due to an immunoglobulin G4 (IgG4)-associated systemic disease.
autoimmune pancreatitis type 2
60 years) and presenting with abdominal pain, steatorrhea and obstructive jaundice
autoimmune polyendocrine syndrome
autoimmune disease of endocrine system with auto-reactivity against endocrine organs
MeSH: D016884
autoimmune polyendocrine syndrome type 1
autoimmune polyendocrine syndrome that is inherited in an autosomal recessive fashion, which is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs
ICD: E31.0
autoimmune polyendocrine syndrome type 2
autoimmune polyendocrine syndrome that is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. It is more heterogeneous and has not been linked to one gene
ICD: E31.0
Autoimmune polyendocrine syndrome type 3
human disease
autoimmune polyendocrinopathy type 4
human disease
Autoimmune Pulmonary Alveolar Proteinosis
A rare lung disorder characterized by accumulation of surfactant proteins in alveoli due to autoantibodies against GM-CSF. Patients experience progressive dyspnea and are at increased risk for opportunistic infections. Global prevalence is estimated at 1 in 100,000.
ICD: CA61.0MeSH: D011648
autoimmune skin disease
hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the skin and connective tissue
autoimmune thrombocytopenia
human disease
autoimmune thrombocytopenic purpura
primary thrombocytopenia that involves relatively few platelets in blood as a result of autoantibodies
MeSH: D016553
autoinflammation lipodystrophy and dermatosis syndrome
Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation
human disease
autoinflammatory syndrome with immune deficiency
human disease
autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
human disease
autoinflammatory syndrome with skin involvement
human disease
autonomic nervous system disease
human disease
ICD: G90MeSH: D001342
autosomal agammaglobulinemia
group of hereditary diseases in humans
MeSH: C538056
autosomal anomaly
human disease
autosomal dominant Alport syndrome
Alport syndrome that has material -basis in heterozygous mutation in the COL4A3 gene
autosomal dominant aplasia and myelodysplasia
human disease
autosomal dominant centronuclear myopathy
centronuclear myopathy that has material basis in autosomal dominant inheritance
autosomal dominant cerebellar ataxia type I
autosomal dominant cerebellar ataxia type II
human disease
autosomal dominant cerebellar ataxia type III
autosomal dominant cerebellar ataxia type IV
human disease