OBO ID: DOID:0080271
Term Name: nephrotic syndrome type 15 Search Ontology:
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)
OTHER nephrotic syndrome type 15 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MAGI2 Nephrotic syndrome, type 15 617609
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None