Search Ontology:
Human Disease

nephrotic syndrome type 15

Term ID
DOID:0080271
Synonyms
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models