Kidney Tissue Atlas Ontology
686 terms(s) returned
| Term Type: | Record: 651 to 686 of 686 Records | Page: 14 of 14, First Previous Next Last | Show Records Per Page |
- hypertrophic cardiomyopathy
- hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
- hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome
- hyperuricemic nephropathy, familial juvenile type 3
- hyperuricemic nephropathy, familial juvenile type 4
- hypoalphalipoproteinemia
- hypocomplementemic urticarial vasculitis
- hypodermis
- hypoglossia/aglossia
- hypogonadism
- hypogonadotropic hypogonadism
- hypolipoproteinemia (disease)
- hypomagnesemia, seizures, and intellectual disability
- hypomagnesemia, seizures, and intellectual disability 1
- hypomagnesemia, seizures, and intellectual disability 2
- hypoparathyroidism
- hypoparathyroidism-deafness-renal disease syndrome
- hypophosphatemic nephrolithiasis/osteoporosis 1
- hypophosphatemic nephrolithiasis/osteoporosis 2
- hypopituitarism
- hypoplastic
- hypothesis driven investigation
- hypothesis generating investigation
- hypothesis textual entity
- hypotonia-cystinuria syndrome
- hypotonia-cystinuria syndrome type 1
- hypotrichosis-lymphedema-telangiectasia syndrome (grouping)
- hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
- hypouricemia, familial renal, due to tubular hypersecretion
- hypouricemia, hypercalcinuria, and decreased bone density
- hypouricemia, renal 1
- hypouricemia, renal, 2
- hypoxanthine guanine phosphoribosyltransferase partial deficiency
- hypoxanthine-guanine phosphoribosyltransferase deficiency
- hypoxia-induced blood vessel dilation expressed as percent of force at maximum constriction
- hypoxia-inducible factor 1-alpha (human)
