Experimental Factor Ontology
1210 terms(s) returned
Term Type: | Record: 901 to 950 of 1210 Records | Page: 19 of 25, First Previous Next Last | Show Records Per Page |
- autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome
- autoimmune gastritis
- autoimmune glomerulonephritis
- autoimmune hemolytic anemia, cold type
- autoimmune hypoparathyroidism
- autoimmune inner ear disease
- autoimmune interstitial lung disease-arthritis syndrome
- autoimmune lymphoproliferative syndrome
- autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
- autoimmune lymphoproliferative syndrome type 2A
- autoimmune lymphoproliferative syndrome type 2B
- autoimmune lymphoproliferative syndrome type 4
- autoimmune myocarditis
- autoimmune neuropathy
- autoimmune oophoritis
- autoimmune optic neuritis
- autoimmune pancreatitis
- autoimmune polyendocrine syndrome type 1
- autoimmune polyendocrinopathy
- autoimmune primary ovarian failure
- autoimmune pulmonary alveolar proteinosis
- autoimmune retinopathy
- autoimmune thrombocytopenia
- autoimmune thyroid disease, susceptibility to
- autoimmune urticaria
- autoimmune uveitis
- autoimmune vasculitis
- autoimmune/inflammatory optic neuropathy
- autoinflammation with arthritis and dyskeratosis
- autoinflammation with pulmonary and cutaneous vasculitis
- autoinflammation, immune dysregulation, and eosinophilia
- autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation
- autoinflammatory disease, X-linked
- autoinflammatory disease, multisystem, with immune dysregulation, X-linked
- autoinflammatory disease, systemic, with vasculitis
- autoinflammatory syndrome
- autoinflammatory syndrome of childhood
- autoinflammatory syndrome with immunodeficiency
- autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
- autoinflammatory syndrome, familial, Behcet-like
- autoinflammatory syndrome, familial, Behcet-like 1
- autoinflammatory syndrome, familial, X-linked, Behcet-like 2
- autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency
- autonomic nervous system neoplasm
- autonomic neuropathy
- autosomal agammaglobulinemia
- autosomal anomaly
- autosomal dominant Alport syndrome
- autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
- autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation