Kidney Tissue Atlas Ontology
124 terms(s) returned
| Term Type: | Record: 1 to 50 of 124 Records | Page: 1 of 3, First Previous Next Last | Show Records Per Page |
- IGAN1
- IGAN2
- IgA glomerulonephritis
- IgG4-related disease
- IgG4-related kidney disease
- Imerslund-Grasbeck syndrome
- Imerslund-Grasbeck syndrome type 1
- Imerslund-Grasbeck syndrome type 2
- ichthyosis (disease)
- ichthyosis-intellectual disability-dwarfism-renal impairment syndrome
- idiopathic and/or familial pulmonary arterial hypertension
- idiopathic aplastic anemia
- idiopathic inflammatory myopathy
- idiopathic inherited hypercalciuria
- idiopathic membranous glomerulonephritis
- idiopathic nephrotic syndrome
- idiopathic steroid-sensitive nephrotic syndrome
- idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation
- idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis
- idiopathic steroid-sensitive nephrotic syndrome with minimal change
- immune complex mediated vasculitis
- immune deficiency disease
- immune system disease
- immune-complex glomerulonephritis
- immuno-osseous dysplasia
- immunodeficiency disease
- immunodeficiency due to a complement regulatory deficiency
- immunodeficiency due to a genetic complement cascade protein anomaly
- immunodeficiency due to absence of thymus
- immunodeficiency with factor H anomaly
- immunodeficiency-related disorder
- immunoglobulin a vasculitis
- immunoglobulin-mediated membranoproliferative glomerulonephritis
- immunotactoid glomerulopathy
- immunotactoid or fibrillary glomerulopathy
- impaired renal function disease
- impulse control disorder
- in situ carcinoma
- inborn carbohydrate metabolic disorder
- inborn disorder of amino acid absorption and transport
- inborn disorder of amino acid and other organic acid metabolism
- inborn disorder of bilirubin metabolism
- inborn disorder of cobalamin metabolism and transport
- inborn disorder of energy metabolism
- inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation
- inborn disorder of lysosomal amino acid transport
- inborn disorder of methionine cycle and sulfur amino acid metabolism
- inborn disorder of phenylalanin or tyrosine metabolism
- inborn disorder of porphyrin metabolism
- inborn disorder of purine metabolism
