OBO ID: DOID:0080386
Term Name: nephrotic syndrome type 10 Search Ontology:
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:
Ontology: Human Disease   (DOID:0080386)
OTHER nephrotic syndrome type 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
EMP2 Nephrotic syndrome, type 10 615861
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None