Kidney Tissue Atlas Ontology
140 terms(s) returned
Term Type: Class | Record: 101 to 140 of 140 Records | Page: 3 of 3, First Previous Next Last | Show Records Per Page |
- neuroendocrine neoplasm
- neurofaciodigitorenal syndrome
- neurofibromatosis
- neurofibromatosis type 1
- neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
- neurofibromatosis, familial spinal
- neurohypophyseal diabetes insipidus
- neurometabolic disease
- neuromuscular disease
- neurovascular disease
- neutropenia
- non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature
- non-acquired combined pituitary hormone deficiency
- non-acquired pituitary hormone deficiency
- non-amyloid fibrillary glomerulopathy
- non-amyloid monoclonal immunoglobulin deposition disease
- non-congenital cyst of kidney
- non-familial dilated cardiomyopathy
- non-familial hypertrophic cardiomyopathy
- non-familial rare disease with dilated cardiomyopathy
- non-familial restrictive cardiomyopathy
- non-immune hydrops fetalis
- non-immunoglobulin-mediated membranoproliferative glomerulonephritis
- non-renal secondary hyperparathyroidism
- non-syndromic central nervous system malformation
- non-syndromic developmental defect of the eye
- non-syndromic diaphragmatic or abdominal wall malformation
- non-syndromic renal or urinary tract malformation
- non-syndromic urogenital tract malformation
- non-syndromic urogenital tract malformation of female
- non-syndromic urogenital tract malformation of male and female
- non-syndromic uterovaginal malformation
- nonanaplastic kidney Wilms tumor
- nonpapillary renal cell carcinoma
- noonan syndrome 12
- normocytic anemia
- nose and cavum anomaly
- nutritional deficiency disease
- nutritional disorder
- nutritional or metabolic disease