D	C99102	Glutaric Acidemia Type 2	Glutaric Aciduria, Type 2		A rare autosomal recessive inherited metabolic disorder caused by mutations in the ETFA, ETFB, or ETFDH genes. It is characterized by deficiency of the enzyme electron transfer flavoprotein or the enzyme electron transfer flavoprotein dehydrogenase. It results in metabolic acidosis, hypoglycemia, and behavioral changes. Additional abnormalities include brain malformations, facial malformations, dilated cardiomyopathy, and hepatomegaly.		C34816	Congenital Metabolic Disorder			C90259	Pediatric Terminology	
A	C120893	Hypoplasia	Hypoplasia		Incomplete or underdevelopment of a tissue or organ.	Incomplete or underdevelopment of a tissue or organ.	C3367	Finding			C90259	Pediatric Terminology	
A	C128108	Idiopathic Membranous Glomerulopathy	Idiopathic Membranous Glomerulopathy		Chronic degenerative changes in the kidney characterized by thickened and inflamed glomeruli and proteinurea, the cause of which is unknown.	Membranous glomerulopathy, the cause of which is not known.	C120887	Glomerulopathy			C90259	Pediatric Terminology	
A	C128110	Nephrotic Syndrome - Infrequently Relapsing	Nephrotic Syndrome - Infrequently Relapsing		Nephrotic syndrome in which there is a relapse occuring less than twice in the first six months, or less than four times in a year.	Nephrotic syndrome in which there is a relapse occurring less than twice in the first six months, or less than four times in a year.	C34845	Nephrotic Syndrome			C90259	Pediatric Terminology	
A	C128143	Idiopathic Crescentic Glomerulonephritis	Idiopathic Crescentic Glomerulonephritis		Crescentic glomerulonephritis, the cause of which is unknown.	Crescentic glomerulonephritis, the cause of which is not known.	C35444	Crescentic Glomerulonephritis			C90259	Pediatric Terminology	
A	C128144	Membranous Nephropathy - Secondary	Membranous Nephropathy - Secondary	Secondary Membranous Glomerulopathy	Membranous nephropathy due to another medical condition.	Membranous nephropathy due to another medical condition.	C34645	Membranous Nephropathy			C90259	Pediatric Terminology	
A	C128145	Pierson Syndrome	Pierson Syndrome		An autosomal recessive disorder caused by mutation(s) in the LAMB2 gene, encoding laminin subunit beta-2. It is characterized by congenital nephrotic syndrome with diffuse mesangial sclerosis and distinct ocular abnormalities.	An autosomal recessive disorder caused by mutation(s) in the LAMB2 gene, encoding laminin subunit beta-2. It is characterized by congenital nephrotic syndrome with diffuse mesangial sclerosis and distinct ocular abnormalities.	C35337	Congenital Nephrotic Syndrome			C90259	Pediatric Terminology	
A	C128146	Renal Infarct	Renal Infarct	Kidney Infarct	Ischemic necrosis of the kidney caused by interruption of the blood supply to the area.	Ischemic necrosis of the kidney caused by interruption of the blood supply to the area.	C25738	Infarct			C90259	Pediatric Terminology	
A	C128147	Acquired Solitary Kidney	Acquired Solitary Kidney		A finding of one kidney after the loss of the second, whether due to injury, disease or surgery.	A finding of one kidney after the loss of the second, whether due to injury, disease or surgery.	C36287	Congenital or Acquired Anatomic Abnormality			C90259	Pediatric Terminology	
A	C35444	Crescentic Glomerulonephritis	Crescentic Glomerulonephritis		A histopathologic term for a pattern of diseases characterized by extensive crescent formation in the glomeruli; patients present clinically with rapid deterioration of renal function, and possible progression to end-stage renal failure within weeks or months.	A histopathologic term for a pattern of diseases characterized by extensive crescent formation in the glomeruli; patients present clinically with rapid deterioration of renal function, and possible progression to end-stage renal failure within weeks or months.	C26784	Glomerulonephritis			C90259	Pediatric Terminology	
A	C45435	Secondary Focal Segmental Glomerulosclerosis	Secondary Focal Segmental Glomerulosclerosis	Secondary FSGS	Focal segmental glomerulosclerosis due to another medical condition.	Focal segmental glomerulosclerosis due to another medical condition.	C37308	Focal Segmental Glomerulosclerosis			C90259	Pediatric Terminology	
A	C84907	Multiple Acyl-CoA Dehydrogenase Deficiency	Glutaric Aciduria, Type 2