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Disease association ontology term - MONDO:0012555 - Cornelia de Lange syndrome 3

Term summary

ID
MONDO:0012555
Name
Cornelia de Lange syndrome 3
Ontology or CV name
Disease association
Definition
Any Cornelia de Lange syndrome in which the cause of the disease is a mutation in the SMC3 gene.

Parents

Annotation

Disease association

MONDO:0012555 - Cornelia de Lange syndrome 3

References:

Genes: