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Disease association ontology term - MONDO:0013428 - Meier-Gorlin syndrome 2

Term summary

ID
MONDO:0013428
Name
Meier-Gorlin syndrome 2
Ontology or CV name
Disease association
Definition
Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC4 gene.

Parents

Annotation

Disease association

MONDO:0013428 - Meier-Gorlin syndrome 2

References:

Genes: