PomBase home

Disease association ontology term - MONDO:0008021 - Cowden syndrome 1

Term summary

ID
MONDO:0008021
Name
Cowden syndrome 1
Ontology or CV name
Disease association
Definition
Any Cowden disease in which the cause of the disease is a mutation in the PTEN gene.

Parents

Annotation

Disease association

MONDO:0008021 - Cowden syndrome 1

References:

Genes: