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Disease association ontology term - MONDO:0014802 - Cowden syndrome 7

Term summary

ID
MONDO:0014802
Name
Cowden syndrome 7
Ontology or CV name
Disease association
Definition
Any Cowden disease in which the cause of the disease is a mutation in the SEC23B gene.

Parents

Annotation

Disease association

MONDO:0014802 - Cowden syndrome 7

References:

Genes: