Kidney Tissue Atlas Ontology
124 terms(s) returned
Term Type: Class | Record: 51 to 100 of 124 Records | Page: 2 of 3, First Previous Next Last | Show Records Per Page |
- inborn disorder of purine or pyrimidine metabolism
- inborn errors of metabolism
- inborn metal metabolism disorder
- inborn mitochondrial metabolism disorder
- inborn vitamin B12 deficiency (disease)
- inborn vitamin metabolic disorder
- infantile Bartter syndrome with sensorineural deafness
- infection-related hemolytic uremic syndrome
- infectious disease
- infectious disease characteristic
- infertility disorder
- infiltrating renal pelvis transitional cell carcinoma
- infiltrating renal pelvis/ureter urothelial carcinoma
- infiltrating urothelial carcinoma
- inflammatory and autoimmune disease with epilepsy
- inflammatory disease
- infundibulopelvic stenosis-multicystic kidney syndrome
- inherited
- inherited Fanconi renotubular syndrome
- inherited amino acid metabolic disorder
- inherited aplastic anemia
- inherited auditory system disease
- inherited bleeding disorder, platelet-type
- inherited blood coagulation disorder
- inherited deficiency anemia
- inherited disease susceptibility
- inherited dystonia
- inherited epidermolysis bullosa
- inherited hemoglobinopathy
- inherited ichthyosis
- inherited ichthyosis syndromic form
- inherited lipid metabolism disorder
- inherited nervous system cancer-predisposing syndrome
- inherited neurodegenerative disorder
- inherited neuroendocrine tumor
- inherited non-syndromic ichthyosis
- inherited odontologic disease
- inherited organic acidemia
- inherited paroxysmal nocturnal hemoglobinuria
- inherited primary ovarian failure
- inherited pseudoxanthoma elasticum
- inherited renal cancer-predisposing syndrome
- inherited renal tubular disease
- inherited retinal dystrophy
- inherited skin tumor
- inherited soft tissue tumor
- inherited thrombocytopenia
- inherited tremor disorder
- inherited vitreoretinopathy
- inherited vitreous-retinal disease