Kidney Tissue Atlas Ontology
189 terms(s) returned
Term Type: Class | Record: 101 to 150 of 189 Records | Page: 3 of 4, First Previous Next Last | Show Records Per Page |
- complement deficiency
- complement factor H deficiency
- complex chromosomal rearrangement
- complex hereditary spastic paraplegia
- congenital
- congenital T-cell immunodeficiency
- congenital abnormality
- congenital anemia
- congenital anomalies of kidney and urinary tract 1
- congenital anomalies of kidney and urinary tract 2
- congenital anomalies of kidney and urinary tract 3
- congenital anomaly of cardiovascular system
- congenital anomaly of kidney and urinary tract
- congenital anomaly of the great arteries
- congenital bilateral megacalycosis
- congenital disorder of glycosylation
- congenital disorder of glycosylation type I
- congenital disorder of glycosylation type II
- congenital disorder of glycosylation with cardiac malformation as a major feature
- congenital disorder of glycosylation with developmental anomaly
- congenital disorder of glycosylation with epilepsy as a major feature
- congenital disorder of glycosylation with hepatic involvement
- congenital disorder of glycosylation with intestinal involvement
- congenital disorder of glycosylation with nephropathy as a major feature
- congenital disorder of glycosylation with neurological involvement
- congenital disorder of glycosylation with skin involvement
- congenital entropion
- congenital heart malformation
- congenital hematological disorder
- congenital hydrocephalus
- congenital hydronephrosis
- congenital hypogonadotropic hypogonadism
- congenital hypothalamic hamartoma syndrome
- congenital intestinal transport defect
- congenital limb malformation
- congenital megacalycosis
- congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization
- congenital mesoblastic nephroma
- congenital nephrotic syndrome - interstitial lung disease - epidermolysis bullosa syndrome
- congenital nephrotic syndrome, Finnish type
- congenital nervous system disorder
- congenital or acquired
- congenital primary megaureter
- congenital primary megaureter, nonrefluxing and unobstructed form
- congenital primary megaureter, obstructed form
- congenital primary megaureter, refluxing form
- congenital renal artery stenosis
- congenital sialidosis type 2
- congenital thrombotic thrombocytopenic purpura
- congenital unilateral hypoplasia of depressor anguli oris