Kidney Tissue Atlas Ontology
291 terms(s) returned
| Term Type: | Record: 151 to 200 of 291 Records | Page: 4 of 6, First Previous Next Last | Show Records Per Page |
- familial Mediterranean fever, autosomal dominant
- familial cardiomyopathy
- familial cystic renal disease
- familial dilated cardiomyopathy
- familial gestational hyperthyroidism
- familial hemolytic anemia
- familial hyperaldosteronism
- familial hyperthyroidism due to mutations in TSH receptor
- familial hypertrophic cardiomyopathy
- familial idiopathic steroid-resistant nephrotic syndrome
- familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
- familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
- familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
- familial juvenile hyperuricemic nephropathy
- familial juvenile hyperuricemic nephropathy type 1
- familial juvenile hyperuricemic nephropathy type 2
- familial nephrotic syndrome
- familial nonmedullary thyroid carcinoma
- familial osteosclerosis
- familial papillary thyroid carcinoma with renal papillary neoplasia
- familial primary hyperparathyroidism
- familial primary hypomagnesemia
- familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- familial primary hypomagnesemia with hypocalcuria
- familial primary hypomagnesemia with normocalciuria and normocalcemia
- familial primary hypomagnesemia with normocalcuria
- familial renal glucosuria
- familial restrictive cardiomyopathy
- familial steroid-resistant nephrotic syndrome with sensorineural deafness
- familial syndrome associated with hypertrophic cardiomyopathy
- familial visceral amyloidosis
- familial visceral myopathy
- family status inclusion criterion
- fast-slope measurement of chemical-induced contraction
- fatty acid-binding protein, liver
- fatty acid-binding protein, liver (human)
- feature_attribute
- female
- female gender role
- female infertility
- female infertility due to a congenital hypogonadotropic hypogonadism
- female infertility due to an anomaly of ovarian function
- female infertility due to an anomaly of ovarian function of genetic origin
- female infertility due to an implantation defect
- female infertility due to an implantation defect of genetic origin
- female infertility due to gonadal dysgenesis
- female infertility due to hypothalamic-pituitary-gonadal axis disorder
- female organism
- female pregnancy
- female reproductive organ
