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Disease association ontology term - MONDO:0008869 - Seckel syndrome 1

Term summary

ID
MONDO:0008869
Name
Seckel syndrome 1
Ontology or CV name
Disease association
Definition
Any Seckel syndrome in which the cause of the disease is a mutation in the ATR gene.

Parents

Annotation

Disease association

MONDO:0008869 - Seckel syndrome 1

References:

Genes: