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Human Disease

nephrotic syndrome type 11

Term ID
DOID:0080385
Synonyms
Definition
A familial nephrotic syndrome characterized by onset in the first decade of life of steroid resistant progressive renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NUP107 gene on chromosome 12q15. https://www.ncbi.nlm.nih.gov/pubmed/26411495
References
Ontology
Human Disease   ( DOID:0080385 )
Relationships
is a type of
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Genes Involved
Zebrafish Models