nephrotic syndrome type 10

Term ID

DOID:0080386

Synonyms

Definition

A familial nephrotic syndrome characterized by early childhood onset that has_material_basis_in homozygous or compound heterozygous mutation in the EMP2 gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/24814193

References

• OMIM:615861

Ontology

Human Disease   ( DOID:0080386 )