Kidney Tissue Atlas Ontology
143 terms(s) returned
Term Type: Class | Record: 51 to 100 of 143 Records | Page: 2 of 3, First Previous Next Last | Show Records Per Page |
- median facial cleft
- medullary cystic kidney disease 1
- medullary cystic kidney disease 2
- medullary sponge kidney
- megacystis-megaureter syndrome
- megacystis-microcolon-intestinal hypoperistalsis syndrome
- megaloblastic anemia (disease)
- membranoproliferative glomerulonephritis (disease)
- membranoproliferative glomerulonephritis, X-linked
- membranous glomerulonephritis
- meningoencephalitis
- mental disorder
- mesangial proliferative glomerulonephritis
- mesenchymal cell neoplasm
- mesoblastic nephroma
- mesomelic and rhizo-mesomelic dysplasia
- mesonephric adenocarcinoma
- mesonephric neoplasm
- metabolic disease
- metabolic disease associated with ocular features
- metabolic disease with cataract
- metabolic disease with corneal opacity
- metabolic disease with dementia
- metabolic disease with epilepsy
- metabolic disease with intestinal involvement
- metabolic disease with pigmentary retinitis
- metabolic disease with skin involvement
- metabolic epilepsy
- metachronous kidney Wilms' tumor
- metal transport or utilization disorder with epilepsy
- metanephric adenoma
- methylcobalamin deficiency type cblG
- methylmalonic acidemia
- methylmalonic acidemia without homocystinuria
- methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
- microscopic polyangiitis
- mild phosphoribosylpyrophosphate synthetase superactivity
- mild pre-eclampsia
- mineral metabolism disease
- mitochondrial DNA depletion syndrome
- mitochondrial DNA depletion syndrome, hepatocerebral form
- mitochondrial DNA depletion syndrome, hepatocerebrorenal form
- mitochondrial DNA maintenance syndrome
- mitochondrial disease
- mitochondrial disease with epilepsy
- mitochondrial disease with hypertrophic cardiomyopathy
- mitochondrial disease with peripheral neuropathy
- mitochondrial disorder due to a defect in mitochondrial protein synthesis
- mitochondrial oxidative phosphorylation disorder
- mitochondrial oxidative phosphorylation disorder due to a duplication of mitochondrial DNA