Search Ontology:
Human Disease
nephrotic syndrome type 15
- Term ID
- DOID:0080271
- Synonyms
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- Definition
- A familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the MAGI2 gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/27932480
- References
- Ontology
- Human Disease ( DOID:0080271 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models