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Disease association ontology term - MONDO:0015026 - cerebroretinal microangiopathy with calcifications and cysts 2

Term summary

ID
MONDO:0015026
Name
cerebroretinal microangiopathy with calcifications and cysts 2
Ontology or CV name
Disease association
Definition
Any Coats plus syndrome in which the cause of the disease is a mutation in the STN1 gene.

Parents

Annotation

Disease association

MONDO:0015026 - cerebroretinal microangiopathy with calcifications and cysts 2

References:

Genes: