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

• OMIM:617609

Ontology

Human Disease   ( DOID:0080271 )