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Disease association ontology term - MONDO:0014752 - nephrotic syndrome, type 11

Term summary

ID
MONDO:0014752
Name
nephrotic syndrome, type 11
Ontology or CV name
Disease association
Definition
Any familial nephrotic syndrome in which the cause of the disease is a mutation in the NUP107 gene.

Parents

Annotation

Disease association

MONDO:0014752 - nephrotic syndrome, type 11

References:

Genes: