Experimental Factor Ontology
3808 terms(s) returned
| Term Type: Class | Record: 3451 to 3500 of 3808 Records | Page: 70 of 77, First Previous Next Last | Show Records Per Page |
- autoimmune neuropathy
- autoimmune oophoritis
- autoimmune optic neuritis
- autoimmune pancreatitis
- autoimmune pancreatitis type 1
- autoimmune polyendocrine syndrome type 1
- autoimmune polyendocrinopathy
- autoimmune primary ovarian failure
- autoimmune pulmonary alveolar proteinosis
- autoimmune retinopathy
- autoimmune thrombocytopenia
- autoimmune thrombocytopenic purpura
- autoimmune thyroid disease
- autoimmune thyroid disease, susceptibility to
- autoimmune type 1 diabetes
- autoimmune urticaria
- autoimmune uveitis
- autoimmune vasculitis
- autoimmune/inflammatory optic neuropathy
- autoinflammation with arthritis and dyskeratosis
- autoinflammation with episodic fever and lymphadenopathy
- 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 dysreflexia
- autonomic nervous system
- autonomic nervous system disease
- autonomic nervous system neoplasm
- autonomic neuropathy
- autophagy protein 5
- autopod
- 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
- autosomal dominant Charcot-Marie-Tooth disease type 2K
- autosomal dominant Charcot-Marie-Tooth disease type 2M
- autosomal dominant Charcot-Marie-Tooth disease type 2W
