Kidney Tissue Atlas Ontology
101 terms(s) returned
Term Type: Class | Record: 51 to 100 of 101 Records | Page: 2 of 3, First Previous Next Last | Show Records Per Page |
- disease of glomerular basement membrane
- disease of macromolecular complex
- disease of membrane bound organelle
- disease of orbital region
- disease of pilosebaceous unit
- disease of retroperitoneum
- disease of signal transduction
- disease of supramolecular complex
- disease of transporter activity
- disease of visual system
- disease or disorder
- disease susceptibility
- disorder by anatomical region
- disorder of GPI anchor biosynthesis
- disorder of O-xylosylglycan synthesis
- disorder of acid-base balance
- disorder of carbohydrate absorption and transport
- disorder of copper metabolism
- disorder of development or morphogenesis
- disorder of fructose metabolism
- disorder of galactose metabolism
- disorder of glycosylation
- disorder of glyoxylate metabolism
- disorder of magnesium transport
- disorder of metabolite absorption and transport
- disorder of mineral absorption and transport
- disorder of multiple glycosylation
- disorder of neutral amino acid transport
- disorder of organic acid metabolism
- disorder of peroxisomal alpha-, beta- and omega-oxidation
- disorder of phospholipids, sphingolipids and fatty acids biosynthesis
- disorder of protein N-glycosylation
- disorder of protein O-glycosylation
- disorder of tyrosine metabolism
- disorder of vitamin and non-protein cofactor absorption and transport
- disorder of zinc metabolism
- distal arthrogryposis
- distal renal tubular acidosis (disease)
- dominant beta-thalassemia
- dominant hypophosphatemia with nephrolithiasis or osteoporosis
- double uterus-hemivagina-renal agenesis syndrome
- drug-related renal tubular dysgenesis
- duplication of urethra
- dyschondrosteosis-nephritis syndrome
- dysentery
- dysostosis
- dysostosis of genetic origin
- dysostosis of genetic origin with limb anomaly as a major feature
- dysostosis with limb and face anomalies as a major feature
- dysostosis with limb anomaly as a major feature