Kidney Tissue Atlas Ontology
50 terms(s) returned
| Term Type: | Record: 1 to 50 of 50 Records | Page: 1 of 1, First Previous Next Last | Show Records Per Page |
- DNA repair disease
- Deal Barratt Dillon syndrome
- Dent disease
- Dent disease type 1
- Dent disease type 2
- dense deposit disease
- dermis disorder
- developmental anomaly of metabolic origin
- developmental defect during embryogenesis
- developmental disorder of mental health
- diabetes insipidus
- diabetes insipidus, nephrogenic, X-linked
- diabetes insipidus, nephrogenic, autosomal
- diabetes mellitus
- diabetic kidney disease
- diffuse glomerulonephritis
- digenic Alport syndrome
- digestive system disorder
- dipsogenic diabetes insipidus
- disease
- disease by body system or component
- disease by developmental or physiological process
- disease by etiologic mechanism
- disease by molecular mechanism
- disease characteristic
- disease has major feature
- disease has primary infectious agent
- disease of genetic or genomic mechanism
- disease of primarily extrinsic mechanism
- disease susceptibility
- disease_has_basis_in_development_of
- disorder of GNAS inactivation
- disorder of GPI anchor biosynthesis
- disorder of acid-base balance
- disorder of carbohydrate transmembrane transport and absorption
- disorder of development or morphogenesis
- disorder of glycolysis
- disorder of glycosylation
- disorder of magnesium transport
- disorder of metabolite absorption and transport
- disorder of mineral absorption and transport
- disorder of orbital region
- disorder of peptide and amine metabolism
- disorder of phospholipids, sphingolipids and fatty acids biosynthesis
- disorder of visual system
- disorder of zinc metabolism
- distal renal tubular acidosis
- drug-related renal tubular dysgenesis
- duplication of urethra
- dysostosis
