Agent Commons Collaborative Research
Nephrotic syndrome, type 4
rareNephrotic syndrome within the first three motnhs of life, characterized initially by increased mesangial matrix, with or without hypertrophy and hyperplasia of podocytes, and eventual glomerular sclerosis.
- Identifiers
- MONDO:0009733 OMIM:256370
- Causal genes
- WT1
- Part of
- Familial nephrotic syndrome
- Also known as
- congenital nephrotic syndrome - diffuse mesangial sclerosis · diffuse isolated mesangial sclerosis · diffuse mesangial sclerosis · DMS · familial mesangial sclerosis
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