Human Disease Ontology
2240 terms(s) returned
| Term Type: | Record: 1601 to 1650 of 2240 Records | Page: 33 of 45, First Previous Next Last | Show Records Per Page |
- autoimmune disease of skin and connective tissue
- autoimmune disease of the nervous system
- autoimmune disease of urogenital tract
- autoimmune epilepsy
- autoimmune gastritis
- autoimmune glomerulonephritis
- autoimmune hemolytic anemia
- autoimmune hepatitis
- autoimmune interstitial lung, joint, and kidney disease
- autoimmune lymphoproliferative syndrome
- autoimmune lymphoproliferative syndrome type 2A
- autoimmune lymphoproliferative syndrome type 2B
- autoimmune lymphoproliferative syndrome type 3
- autoimmune lymphoproliferative syndrome type 4
- autoimmune myocarditis
- autoimmune neuropathy
- autoimmune optic neuritis
- autoimmune pancreatitis
- autoimmune peripheral neuropathy
- autoimmune polyendocrine syndrome
- autoimmune polyendocrine syndrome type 1
- autoimmune polyendocrine syndrome type 2
- autoimmune thrombocytopenic purpura
- autoimmune thyroiditis
- autoimmune uveitis
- autoimmune vasculitis
- autoinflammation, antibody deficiency, and immune dysregulation syndrome
- autoinflammation, panniculitis, and dermatosis syndrome
- autoinflammatory disease
- autoinflammatory syndrome with cytopenia, hyperzincemia, and hypercalprotectinemia
- autonomic nervous system
- autonomic nervous system benign neoplasm
- autonomic nervous system disease
- autonomic nervous system neoplasm
- autonomic neuropathy
- autonomic peripheral neuropathy
- autopod bone
- autopod endochondral element
- autopod region
- autopodial extension
- autosomal dominant Aarskog syndrome
- autosomal dominant Emery-Dreifuss muscular dystrophy 2
- autosomal dominant Emery-Dreifuss muscular dystrophy 4
- autosomal dominant Emery-Dreifuss muscular dystrophy 5
- autosomal dominant Emery-Dreifuss muscular dystrophy 7
- autosomal dominant Robinow syndrome 1
- autosomal dominant Robinow syndrome 2
- autosomal dominant Robinow syndrome 3
- autosomal dominant Wolfram syndrome
- autosomal dominant adult-onset proximal spinal muscular atrophy
