Search Ontology:
Human Disease
nephrotic syndrome type 21
- Term ID
- DOID:0112267
- Synonyms
-
- NPHS21
- Definition
- A familial nephrotic syndrome characterized by onset of rapidly, progressive kidney dysfunction in the first year of life, proteinuria, and diffuse mesangial sclerosis that has_material_basis_in homozygous or compound heterozygous mutation in the AVIL gene on chromosome 12q14.1. https://pubmed.ncbi.nlm.nih.gov/29058690/
- References
- Ontology
- Human Disease ( DOID:0112267 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models