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Disease association ontology term - MONDO:0009039 - Baller-Gerold syndrome

Term summary

ID
MONDO:0009039
Name
Baller-Gerold syndrome
Ontology or CV name
Disease association
Definition
Baller-Gerold syndrome is characterized by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius).

Parents

Annotation

Disease association

MONDO:0009039 - Baller-Gerold syndrome

References:

Genes: