Kidney Tissue Atlas Ontology
478 terms(s) returned
Term Type: Class | Record: 351 to 400 of 478 Records | Page: 8 of 10, First Previous Next Last | Show Records Per Page |
- neurofibromatosis type 1
- neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
- neurofibromatosis, familial spinal
- neurogenic placode
- neurohypophyseal diabetes insipidus
- neurohypophysis
- neurometabolic disease
- neuromuscular disease
- neuromuscular process
- neuron
- neuron associated cell
- neuron projection
- neuron projection bundle
- neuron projection bundle
- neuronal membrane glycoprotein M6-a (human)
- neurosurgereon role
- neurotoxin
- neurovascular disease
- neurula stage
- neutral amino acid transport
- neutropenia
- neutrophil
- neutrophil gelatinase-associated lipocalin (human)
- neutrophillic
- neutrophillic cytoplasm
- neutrophillic cytoplasm
- new patient form
- nitric-oxide synthase biosynthetic process
- nitrogen atom
- nitrogen compound metabolic process
- nitrogen compound transport
- nitrogen hydride
- nitrogen molecular entity
- no answer to question
- no formal school education level
- no insurance status
- 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-branched duct epithelial cell
- non-congenital cyst of kidney
- non-connected functional system
- non-familial dilated cardiomyopathy
- non-familial hypertrophic cardiomyopathy
- non-familial rare disease with dilated cardiomyopathy
- non-familial restrictive cardiomyopathy
- non-functional
- non-hospital institution visit