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Disease association ontology term - MONDO:0014817 - nephrotic syndrome, type 12

Term summary

ID
MONDO:0014817
Name
nephrotic syndrome, type 12
Ontology or CV name
Disease association
Definition
Any familial nephrotic syndrome in which the cause of the disease is a mutation in the NUP93 gene.

Parents

Annotation

Disease association

MONDO:0014817 - nephrotic syndrome, type 12

References:

Genes: