Search Ontology:
Human Disease

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
Ontology
Human Disease   ( DOID:0080386 )
Relationships
is a type of
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Genes Involved
Zebrafish Models