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Disease association ontology term - MONDO:0011715 - Seckel syndrome 2

Term summary

ID
MONDO:0011715
Name
Seckel syndrome 2
Ontology or CV name
Disease association
Definition
Any Seckel syndrome in which the cause of the disease is a mutation in the RBBP8 gene.

Parents

Annotation

Disease association

MONDO:0011715 - Seckel syndrome 2

References:

Genes: