Kidney Tissue Atlas Ontology
11852 terms(s) returned
| Term Type: | Record: 4801 to 4850 of 11852 Records | Page: 97 of 238, First Previous Next Last | Show Records Per Page |
- atypical hemolytic-uremic syndrome with MCP/CD46 anomaly
- atypical hemolytic-uremic syndrome with anti-factor H antibodies
- atypical hemolytic-uremic syndrome with thrombomodulin anomaly
- atypical hypotonia-cystinuria syndrome
- auditory system
- auditory system disease
- author information textual entity
- autoimmune cardiomyopathy
- autoimmune disease
- autoimmune disease of blood
- autoimmune disease of cardiovascular system
- autoimmune disease of central nervous system
- autoimmune disease of ear, nose and throat
- autoimmune disease of endocrine system
- autoimmune disease of musculoskeletal system
- autoimmune disease of peripheral nervous system
- autoimmune disease of the nervous system
- autoimmune disease of urogenital tract
- autoimmune disease with skin involvement
- autoimmune glomerulonephritis
- autoimmune interstitial lung disease-arthritis syndrome
- autoimmune neuropathy
- autoimmune retinopathy
- autoimmune thrombocytopenia
- autoimmune thrombocytopenic purpura
- autoimmune vasculitis
- autoinflammatory syndrome
- autoinflammatory syndrome with immune deficiency
- autoinflammatory syndrome with skin involvement
- autopod bone
- autopod cartilage
- autopod endochondral element
- autopod joint
- autopod region
- autopodial extension
- autopodial skeleton
- autosomal anomaly
- autosomal dominant Alport syndrome
- autosomal dominant complex spastic paraplegia
- autosomal dominant disease
- autosomal dominant distal renal tubular acidosis
- autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome
- autosomal dominant intermediate Charcot-Marie-Tooth disease
- autosomal dominant medullary cystic kidney disease with hyperuricemia
- autosomal dominant medullary cystic kidney disease with or without hyperuricemia
- autosomal dominant polycystic kidney disease
- autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
- autosomal dominant progressive nephropathy with hypertension
- autosomal dominant proximal renal tubular acidosis
- autosomal dominant pseudohypoaldosteronism type 1
